Startseite Crystal structure of 2-(5-ethylpyridin-2-yl)ethyl 2-(6-methoxynaphthalen-2-yl)propanoate, C23H25NO3
Artikel Open Access

Crystal structure of 2-(5-ethylpyridin-2-yl)ethyl 2-(6-methoxynaphthalen-2-yl)propanoate, C23H25NO3

  • Rui Li ORCID logo , Yang Liu , Yue-Yao Jiang und Dong-Li Jiang ORCID logo EMAIL logo
Veröffentlicht/Copyright: 15. April 2024

Abstract

C23H25NO3, monoclinic, P21 (no. 4), a = 15.2433(7) Å, b = 5.8687(3) Å, c = 22.3558(11) Å, β = 105.461(2)°, V = 1927.54(16) Å3, Z = 4, R gt(F) = 0.0413, wR ref(F 2) = 0.1055, T = 100(2) K.

CCDC no.: 2343307

The molecular structure is shown in the figure. Table 1 contains crystallographic data and Table 2 contains the list of the atoms including atomic coordinates and displacement parameters.

Table 1:

Data collection and handling.

Crystal: Colourless block
Size: 0.12 × 0.11 × 0.10 mm
Wavelength: MoKα radiation (0.71073 Å)
μ: 0.08 mm−1
Diffractometer, scan mode: Bruker APEX-II, φ and ω
θ max, completeness: 27.7°, >99 %
N(hkl)measured, N(hkl)unique, R int: 71,927, 8918, 0.046
Criterion for I obs, N(hkl)gt: I obs > 2 σ(I obs), 8051
N(param)refined: 493
Programs: Bruker [1], Olex2 [2], Shelx [3]
Table 2:

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2).

Atom x y z U iso*/U eq
C1 0.06837 (18) 1.6084 (5) 0.95343 (12) 0.0324 (6)
H1A 0.033347 1.621226 0.909913 0.049*
H1B 0.113271 1.731650 0.963496 0.049*
H1C 0.027089 1.619531 0.980240 0.049*
C2 0.11720 (17) 1.3793 (5) 0.96378 (11) 0.0276 (6)
H2A 0.151955 1.367209 1.007907 0.033*
H2B 0.071278 1.255867 0.955131 0.033*
C3 0.18175 (15) 1.3453 (4) 0.92336 (10) 0.0215 (5)
C4 0.25403 (16) 1.4931 (4) 0.92606 (10) 0.0225 (5)
H4 0.264981 1.616978 0.954451 0.027*
C5 0.31011 (16) 1.4588 (4) 0.88706 (10) 0.0208 (5)
H5 0.360209 1.557485 0.889012 0.025*
C6 0.29215 (15) 1.2781 (4) 0.84498 (10) 0.0200 (5)
C8 0.17068 (16) 1.1671 (5) 0.88081 (11) 0.0244 (5)
H8 0.122346 1.062963 0.879048 0.029*
C9 0.34953 (17) 1.2356 (4) 0.80041 (11) 0.0229 (5)
H9A 0.310253 1.235428 0.757287 0.027*
H9B 0.394876 1.359263 0.804209 0.027*
C10 0.39778 (16) 1.0095 (4) 0.81446 (10) 0.0213 (5)
H10A 0.435649 1.006307 0.857962 0.026*
H10B 0.352880 0.884018 0.808619 0.026*
C11 0.50806 (15) 0.7960 (4) 0.78198 (10) 0.0193 (5)
C12 0.56224 (15) 0.7744 (4) 0.73406 (10) 0.0193 (5)
H12 0.590414 0.925765 0.730292 0.023*
C13 0.63886 (16) 0.5999 (5) 0.75534 (11) 0.0274 (5)
H13A 0.681518 0.652910 0.793793 0.041*
H13B 0.671098 0.582179 0.723104 0.041*
H13C 0.613038 0.453038 0.762742 0.041*
C14 0.44808 (15) 0.5073 (4) 0.66278 (10) 0.0182 (4)
H14 0.452165 0.410014 0.697370 0.022*
C15 0.49834 (14) 0.7139 (4) 0.67096 (10) 0.0167 (4)
C16 0.49061 (14) 0.8549 (4) 0.62069 (10) 0.0159 (4)
H16 0.522608 0.995595 0.626147 0.019*
C17 0.43597 (14) 0.7951 (4) 0.56094 (10) 0.0145 (4)
C18 0.38717 (14) 0.5859 (4) 0.55250(9) 0.0142 (4)
C19 0.39357 (15) 0.4460 (4) 0.60554 (10) 0.0172 (4)
H19 0.359700 0.308296 0.601310 0.021*
C20 0.43177 (14) 0.9341 (4) 0.50789 (10) 0.0165 (4)
H20 0.461538 1.077825 0.512993 0.020*
C21 0.38556 (14) 0.8633 (4) 0.44995 (10) 0.0174 (4)
H21 0.385423 0.954999 0.414903 0.021*
C22 0.33760 (14) 0.6529 (4) 0.44177 (10) 0.0162 (4)
C23 0.33622 (14) 0.5186 (4) 0.49179 (10) 0.0160 (4)
H23 0.301621 0.381838 0.486067 0.019*
C24 0.25315 (16) 0.3843 (4) 0.36967 (10) 0.0210 (5)
H24A 0.228742 0.361848 0.324867 0.032*
H24B 0.203353 0.377706 0.389741 0.032*
H24C 0.297506 0.264282 0.386623 0.032*
C25 0.5923 (2) 0.5174 (6) 0.99068 (14) 0.0382 (7)
H25A 0.593639 0.664498 0.970208 0.057*
H25B 0.647422 0.500637 1.024981 0.057*
H25C 0.538591 0.510260 1.006852 0.057*
C26 0.58800 (15) 0.3270 (5) 0.94433 (11) 0.0236 (5)
H26A 0.534892 0.353873 0.908352 0.028*
H26B 0.577264 0.181905 0.963850 0.028*
C27 0.67177 (15) 0.2991 (4) 0.92058 (10) 0.0180 (5)
C28 0.73496 (15) 0.4704 (4) 0.92229 (11) 0.0214 (5)
H28 0.727781 0.614643 0.939669 0.026*
C29 0.80912 (15) 0.4299 (4) 0.89837 (11) 0.0202 (4)
H29 0.851670 0.547687 0.897868 0.024*
C30 0.81998 (15) 0.2148 (4) 0.87526 (10) 0.0194 (5)
C32 0.68804 (16) 0.0924 (4) 0.89557 (11) 0.0236 (5)
H32 0.644793 −0.025816 0.893681 0.028*
C33 0.89934 (16) 0.1575 (4) 0.84941 (11) 0.0228 (5)
H33A 0.940216 0.290927 0.853307 0.027*
H33B 0.934565 0.029625 0.873092 0.027*
C34 0.86379 (16) 0.0918 (5) 0.78196 (11) 0.0247 (5)
H34A 0.822062 −0.039721 0.778441 0.030*
H34B 0.828725 0.220623 0.758657 0.030*
C35 0.96799 (16) −0.1830 (4) 0.76251 (10) 0.0207 (5)
C36 1.03660 (15) −0.2296 (4) 0.72529 (10) 0.0189 (5)
H36 1.070573 −0.085533 0.722920 0.023*
C37 1.10484 (17) −0.4122 (5) 0.75617 (11) 0.0301 (6)
H37A 1.140584 −0.357599 0.796789 0.045*
H37B 1.145629 −0.445192 0.729996 0.045*
H37C 1.072167 −0.551234 0.761573 0.045*
C38 0.93283 (15) −0.5026 (4) 0.64924 (10) 0.0177 (4)
H38 0.934799 −0.601855 0.683141 0.021*
C39 0.98212 (14) −0.2945 (4) 0.65986 (10) 0.0158 (4)
C40 0.97825 (14) −0.1512 (4) 0.61065 (10) 0.0150 (4)
H40 1.010390 −0.010796 0.617538 0.018*
C41 0.92697 (14) −0.2093 (4) 0.54953 (10) 0.0137 (4)
C42 0.87882 (14) −0.4190 (4) 0.53896 (9) 0.0142 (4)
C43 0.88241(14) −0.5627 (4) 0.59088 (10) 0.0162 (4)
H43 0.849478 −0.702028 0.585036 0.019*
C44 0.92538 (14) −0.0663 (4) 0.49793 (10) 0.0158 (4)
H44 0.955210 0.077218 0.504460 0.019*
C45 0.88137 (15) −0.1333 (4) 0.43903 (10) 0.0167 (4)
H45 0.882711 −0.038329 0.404871 0.020*
C46 0.83362 (14) −0.3437 (4) 0.42847 (10) 0.0159 (4)
C47 0.83042 (14) −0.4827 (4) 0.47734 (10) 0.0156 (4)
H47 0.796267 −0.620148 0.470178 0.019*
C48 0.74854 (17) −0.6034 (4) 0.35303 (11) 0.0237 (5)
H48A 0.729016 −0.624616 0.307933 0.036*
H48B 0.695207 −0.605776 0.369657 0.036*
H48C 0.790142 −0.726629 0.371898 0.036*
N1 0.22323 (14) 1.1317 (4) 0.84210 (9) 0.0242 (4)
N2 0.75986 (15) 0.0460 (4) 0.87386 (10) 0.0263 (5)
O1 0.45483 (11) 0.9825 (3) 0.77199 (7) 0.0216 (4)
O2 0.51064 (12) 0.6639 (3) 0.82377 (8) 0.0269 (4)
O3 0.29660 (10) 0.6014 (3) 0.38101 (7) 0.0194 (3)
O4 0.93732 (11) 0.0324 (3) 0.75463 (7) 0.0225 (4)
O5 0.94111 (14) −0.3212 (3) 0.79315 (8) 0.0343 (4)
O6 0.79413 (10) −0.3892 (3) 0.36703 (7) 0.0204 (3)

1 Source of materials

Naproxen acylchloride was synthesized according to the literature method [4]. 5-Ethyl-2-pyridineethanol (0.01 mol, 1.51 g) and 4-(dimethylamino)-pyridin (DMAP, 0.0015 mol, 0.18 g) were dissolved in dry tetrahydrofuran (20 mL) and triethylamine (0.015 mol, 2 mL). The solution of naproxen acylchloride in dry tetrahydrofuran was dropwise added at 0 °C. The reaction mixture was stirred for 2 h at room temperature. The reaction mixture was filtrated to remove the solid and the filtrate was concentrated under vacuum to remove the solvent. The residue was dissolved in dichloromethane, successively washed with 5 % NaOH solution and water to pH = 7, and dried with anhydrous Na2SO4. The solution was filtrated, and concentrated under vacuum to obtain crude product. The crude product was purified by recrystallization in ethanol. The single crystals were obtained from tetrahydrofuran solution.

2 Experimental details

H atoms were set to calculated positions. The U iso values were set to be 1.5U eq of the carrier atom for methyl H atoms and 1.2U eq for the remaining H atoms.

3 Comment

Naproxen is one of the strongest non-steroidal anti-inflammatory drugs (NSAIDs), inhibits the cyclooxygenase (COX) enzymes both COX-1 and COX-2. Inhibits both COX-1 and COX-2 which are the enzymes of cyclooxygenase (COX). Naproxen displays analgesic, anti-inflammatory, and antipyretic activity. In addition, the researchers reported anticancer l activities of naproxen derivatives [5]. In cure of advancing prostate cancer, naproxen was discovered to be reliable and effective with early repetitive disease in a phase II clinical trial [6]. And naproxen and its derivatives have been shown to be effective as well as other NSAIDs to prevent urinary bladder cancer. By inducing apoptosis and cell cycle arrest toward bladder cancer cells, naproxen displayed anticancer influences. Naproxen inhibited protein kinase B (AKT) phosphorylation and induced apoptosis in rat urinary bladder cancers [7]. In order to achieve high efficiency, low toxicity and cost anti-tumor drugs, we chose naproxen as a core compound and modify its structures.

The compound contains two twist 2-(5-ethylpyridin-2-yl)ethyl 2-(6-methoxynaphthalen-2-yl)propanoate molecules in the asymmetric unit (see Figure). The title compound contained one pyridine ring and one naphthyl moiety. The C=O double bond lengths in the independent molecule are 1.207(3) Å (C11=O2) and 1.202(3) Å (C35=O5), respectively, exhibiting the double bond character. The dihedral angles of ring 1 (C3–C4–C5–C6–N1–C8) and ring 2 (C14–C15–C16–C17–C18–C19), ring 1 (C3–C4–C5–C6–N1–C8) and ring 3 (C17–C18–C23–C22–C21–C20), ring 2 (C14–C15–C16–C17–C18–C19) and ring 3 (C17–C18–C23–C22–C21–C20), ring 4 (C27–C28–C29–C30–N2–C32) and ring 5 (C38–C39–C40–C41–C42–C43), ring 4 (C27–C28–C29–C30–N2–C32) and ring 6 (C42–C41–C44–C45–C46–C47), ring 5 (C38–C39–C40–C41–C42–C43) and ring 6 (C42–C41–C44–C45–C46–C47) are 52.2°, 55.0°, 4.6°, 75.6°, 72.1°, 3.5°, respectively. The other bond distances and angles are in their normal ranges according to the previously reported compounds [8, 9].


Corresponding author: Dong-Li Jiang, China-Japan Union Hospital of Jilin University, Changchun 130021, China, E-mail:

  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: None declared.

  3. Conflict of interest statement: The authors declare no conflicts of interest regarding this article.

References

1. Bruker. Saint and Sadabs; Bruker AXS Inc.: Madison, Wisconsin, USA, 2000.Suche in Google Scholar

2. Dolomanov, O. V., Bourhis, L. J., Gildea, R. J., Howard, J. A. K., Puschmann, H. OLEX2: a complete structure solution, refinement and analysis program. J. Appl. Crystallogr. 2009, 42, 339–341; https://doi.org/10.1107/s0021889808042726.Suche in Google Scholar

3. Sheldrick, G. M. Crystal structure refinement with SHELXL. Acta Crystallogr 2015, C71, 3–8; https://doi.org/10.1107/s2053229614024218.Suche in Google Scholar

4. Huang, Z., Velázquez, C. A., Abdellatif, K. R. A., Chowdhury, M. A., Reisz, J. A., DuMond, J. F., King, S. B., Knaus, E. E. Ethanesulfohydroxamic acid ester prodrugs of nonsteroidal anti-inflammatory drugs (NSAIDs): synthesis, nitric oxide and nitroxyl release, cyclooxygenase inhibition, anti-inflammatory, and ulcerogenicity index studies. J. Med. Chem. 2011, 54, 1356–1364; https://doi.org/10.1021/jm101403g.Suche in Google Scholar PubMed

5. Han, M. I., Kucukguzel, S. G. Anticancer and antimicrobial activities of naproxen and naproxen derivatives. Mini Rev. Med. Chem. 2020, 20, 1300–1310; https://doi.org/10.2174/1389557520666200505124922.Suche in Google Scholar PubMed

6. Srinivas, S., Feldman, D. A phase II trial of calcitriol and naproxen in recurrent porstate cancer. Anticancer Res. 2009, 29, 3605–3610.Suche in Google Scholar

7. Kim, M. S., Kim, J. E., Lim, D. Y., Huang, Z., Chen, H., Langfald, A., Lubet, R. A., Grubbs, C. J., Dong, Z., Bode, A. M. Naproxen induces cell cycle arrest and apoptosis in human urinary bladder cancer cell lines and chemically induced cancers by targeting P13-K. Canc. Prev. Res. 2014, 7, 236–245; https://doi.org/10.1158/1940-6207.capr-13-0288.Suche in Google Scholar PubMed PubMed Central

8. Wang, L. L., Xue, D. D. Crystal structure of 3-phenylpropyl 2-(6-methoxynaphthalen-2-yl)propanpate, C23H24O3. Z. Kristallogr. N. Cryst. Struct. 2022, 237, 517–519; https://doi.org/10.1515/ncrs-2022-0114.Suche in Google Scholar

9. Liang, D., Yang, X. H., Sun, W., Wang, W. N., Yang, J. Z., Liu, Y. Y., Wang, G. S. Synthesis, crystal structure and biological activities of naproxen-eugenol ester progrug. Chem. Res. Chinese Univ. 2013, 29, 245–248; https://doi.org/10.1007/s40242-013-2266-9.Suche in Google Scholar

Received: 2024-02-21
Accepted: 2024-03-27
Published Online: 2024-04-15
Published in Print: 2024-06-25

© 2024 the author(s), published by De Gruyter, Berlin/Boston

This work is licensed under the Creative Commons Attribution 4.0 International License.

Artikel in diesem Heft

  1. Frontmatter
  2. New Crystal Structures
  3. The crystal structure of tris((Z)-2-hydroxy-N-((E)-pyridin-2-ylmethylene)benzohydrazonato-k2O,N)europium(III), C39H30N9O6Eu
  4. Crystal structure of (E)-3-(benzylideneamino)-2-phenylthiazolidin-4-one, C16H14N2OS
  5. The crystal structure of (E)-4-fluoro-N′-(1-(o-tolyl)ethylidene)benzohydrazide, C16H15FN2O
  6. Crystal structure of (6-chloropyridin-3-yl)methyl 2-(6-methoxynaphthalen-2-yl)propanoate, C20H18ClNO3
  7. Crystal structure of methyl 3-methoxy-4-(2-methoxy-2-oxoethoxy)benzoate, C12H14O6
  8. The crystal structure of bis[(4-methoxyphenyl)(picolinoyl)amido-κ2 N:N′]copper(II), C26H22CuN4O4
  9. The crystal structure of poly[di(μ2-aqua)-diaqua-bis(3-aminopyridine-4-carboxylate-κ2 O: O′)-tetra(μ2-3-aminopyridine-4-carboxylate-κ2 O: O′)-dineodymium(III), [Nd2(C6H5N2O2)6(H2O)4] n
  10. The crystal structure of t-butyl 7-[3-(4-fluorophenyl)-1-(propan-2-yl)-1H-indol-2-yl]-3,5-dihydroxyhept-6-enoate, C28H34FNO4
  11. Crystal structure of catena-poly[(benzylamine-κ1 N)-(sorbato-κ1 O)-(μ2-sorbato-κ2 O,O′)-copper(II), C19H23CuNO4
  12. Crystal structure of (4-(2-chlorophenyl)-1H-pyrrol-3-yl)(ferrocenyl) methanone, C21H16ClFeNO
  13. The crystal structure of N-[4-(4-bromophenyl)-1,3-thiazol-2-yl]-3-(2-methylphenyl)-2-sulfanylprop-2-enamide hydrate, C19H17BrN2O2S2
  14. The crystal structure of N′-{5-[2-(2,6-dimethylphenoxy) acetamido]-4-hydroxy-1,6-diphenylhexan-2-yl}-3-methyl-2-(2-oxo-1,3-diazinan-1-yl)butanamide hydrate
  15. Crystal structure of 2-(naphthalen-1-yl)ethyl 2-(6-methoxynaphthalen-2-yl)propanoate, C26H24O3
  16. Crystal structure of naphthalen-1-ylmethyl 2-(6-methoxynaphthalen-2-yl)propanoate, C25H22O3
  17. Crystal structure of poly[diaqua- (μ4-5-(1H-1,2,4-triazol-1-yl)benzene-1,3-dicarboxylato-κ5N:O,O’:O’’:O’’’)calcium(II), C10H9CaN3O6
  18. Crystal structure of (E)-N′-(4-((E)-3-(dimethylamino)acryloyl)-3-hydroxyphenyl)-N, N-dimethylformimidamide, C14H19N3O2
  19. Crystal structure of (E)-3-(dimethylamino)-1-(2-hydroxy-4,6-dimethoxyphenyl)prop-2-en-1-one, C13H17NO4
  20. Crystal structure of (2-chloropyridin-3-yl)methyl-2-(6-methoxynaphthalen-2-yl)propanoate, C20H18ClNO3
  21. The crystal structure of diethyl 4-(3,4-dimethylphenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate, C21H27NO4
  22. Crystal structure of (8R,9S,10R,13S,14S,17S)-17-hydroxy-10,13-dimethyl-17-((4-(2-phenylpropyl)phenyl)ethynyl)-1,2,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-3H-cyclopenta[a]phenanthren-3-one, C36H42O2
  23. Synthesis and crystal structure of 4-(4-cyclopropylnaphthalen-1-yl)-2,4-dihydro-3H-1,2,4-triazole-3-thione, C15H13N3S
  24. Crystal structure of catena-poly[aqua-(2,6-di-(2-pyridyl)-pyridine-κ3 N,N′, N″)(μ2-1,4-naphthalene dicarboxylato-κ2 O,O′)nickel(II)], C27H19NiN3O5
  25. Crystal structure of 3-(diphenylphosphoryl)-3-hydroxy-1-phenylpropan-1-one, C21H19O3P
  26. The crystal structure of R,S-{N-[(2-oxidonaphthalen-1-yl)methylidene]phenylglycinato}divinylsilicon, C23H19NO3Si
  27. The crystal structure of 1,2,4-tris(bromomethyl)benzene, C9H9Br3
  28. Crystal structure of chlorido-[4-(pyridin-2-yl)benzaldehyde-κ2 N,C]-(diethylamine-κ1 N)platinum(II), C16H18ClN2OPt
  29. Crystal structure of 3-(methoxycarbonyl)-1-(4-methoxyphenyl)-2,3,4,9- tetrahydro-1H-pyrido[3,4-b]indol-2-ium chloride hydrate, C40H48Cl2N4O9
  30. The crystal structure of 1-(2-chlorobenzyl)-3-(3-chlorophenyl)urea, C14H12Cl2N2O
  31. Hydrothermal synthesis and crystal structure of aqua-tris(4-acetamidobenzoato-κ2 O,O′)-(1,10-phenanthroline-κ2 N,N′)terbium(III) hydrate C39H36N5O11Tb
  32. The crystal structure of zwitterionic 3-aminoisonicotinic acid, C6H6N2O2
  33. The crystal structure of bis{[monoaqua-μ2-4-[(pyridine-4-carbonyl)-amino]-phthalato-κ3 N:O,O′-(2,2′-bipyridine κ2 N,N′)copper(II)]}decahydrate, C48H56N8O22Cu2
  34. Crystal structure of poly[μ10-4,4′-methylene-bis(oxy)benzoatodipotassium], C15H10K2O6
  35. The crystal structure of catena-poly[[tetraaqua[(μ2-1,4-di(4-methyl-1-imidazolyl)benzene] cobalt(II)]bis(formate)], C16H24CoN4O8
  36. The crystal structure of (E)-2-chloro-5-((2-(nitromethylene)imidazolidin-1-yl)methyl)pyridine, C10H11ClN4O2
  37. The crystal structure of (E)-1-(((2-amino-4,5-dimethylphenyl)iminio)methyl)naphthalen-2-olate, C19H18N2O
  38. Crystal structure of N-(acridin-9-yl)-2-(4-methylpiperidin-1-yl) acetamide monohydrate, C21H25N3O2
  39. The crystal structure of dichlorido-bis(3-methyl-3-imidazolium-1-ylpropionato-κ2 O,O′)-zinc(II), C14H20Cl2N4O4Zn
  40. The crystal structure of 2,8-diethyl-1,3,7,9-tetramethyl-4λ4,5λ4-spiro[dipyrrolo[1,2-c:2′,1′-f][1,3,2]diazaborinine-5,2′-naphtho[1,8-de][1,3,2]dioxaborinine], C25H29BN2O2
  41. The crystal structure of 5-tert-butyl-2-(5-tert-butyl-3-iodo-benzofuran-2-yl)-3-iodobenzofuran, C24H24I2O2
  42. Synthesis and crystal structure of methyl 2-{[4-(4-cyclopropyl-1-naphthyl)-4H-1,2,4-triazole-3-yl]thio} acetate, C18H17N3O2S
  43. The crystal structure of n-propylammonium bis(2,3-dimethylbutane-2,3-diolato)borate-boric acid (1/1), [C3H10N][C12H24BO4]·B(OH)3
  44. Crystal structure of methyl 1-(2-bromophenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate, C19H17BrN2O2
  45. Crystal structure of (4-bromobenzyl)triphenylphosphonium bromide ethanol solvate, C52H48Br4OP2
  46. The crystal structure of unsymmetrical BOPHY C26H27BN4
  47. The crystal structure of Tb3B5O11(OH)2
  48. The crystal structure of (Z)-4-ethyl-2-((4-ethyl-3,5-dimethyl-1H-pyrrol-2-yl)methylene)-3,5-dimethyl-2H-pyrrol-1-ium 2,2'-spirobi[naphtho[1,8-de][1,3,2]dioxaborinin]-2-uide, C37H37BN2O4
  49. Crystal structure of bis(methylammonium) hexadecaselenidopalladate(II), (CH3NH3)2PdSe16
  50. The crystal structure of (2-diphenylphosphanylphenyl) 2-[7-(dimethylamino)-2-oxochromen-4-yl]acetate, C31H26NO4P
  51. Crystal structure of (E)-6-(4-ethylpiperazin-1-yl)-2-(3-fluorobenzylidene)-3,4-dihydronaphthalen-1(2H)-one, C23H25FN2O
  52. The structure of RUB-56, (C6H16N)8 [Si32O64(OH)8]·32 H2O, a hydrous layer silicate (2D-zeolite) that contains microporous levyne-type silicate layers
  53. Crystal structure of 4-amino-3,5-dibromobenzonitrile, C7H4Br2N2
  54. Crystal structure of 2-(naphthalen-1-yl)ethyl 2-acetoxybenzoate, C21H18O4
  55. Single-crystal structure determination of Tm3B12O19(OH)7
  56. Crystal structure determination of NdB3.6O7
  57. The crystal structure of NdB6O8(OH)5·H3BO3
  58. Crystal structure of 2-(5-ethylpyridin-2-yl)ethyl 2-(6-methoxynaphthalen-2-yl)propanoate, C23H25NO3
  59. Crystal structure of N-(1-(3,4-dimethoxyphenyl)-2-methylpropyl)aniline, C18H23NO2
  60. Crystal structure of Ba6Cd12Mn4SiF48
  61. Synthesis and crystal structure of 5-fluoro-1-methyl-2-oxo-3-(2-oxochroman-4-yl)indolin-3-yl acetate, C20H16FNO5
  62. The crystal structure of 6-methacryloylbenzo[d][1,3]dioxol-5-yl 4-nitrobenzenesulfonate, C17H13NO8S
  63. Crystal structure of ethyl 2-(3-benzyl-4-oxo-3,4-dihydrophthalazin-1-yl)- 2,2-difluoroacetate, C19H16F2N2O3
  64. The crystal structure of tetrakis(μ 2-(1H-benzimidazole-2-methoxo-κ2 N,O:O:O)-(n-butanol-κO)-chlorido)-tetranickel(II), C48H68Cl4N8O8Ni4
  65. Synthesis and crystal structure of trans-tetraaqua-bis((1-((7-hydroxy-3-(4-methoxy-3-sulfonatophenyl)-4-oxo-4H-chromen-8-yl)methyl)piperidin-1-ium-4-carbonyl)oxy-κO)zinc(II)hexahydrate, C46H64N2O28S2Zn
  66. The crystal structure of 1-(4-carboxybutyl)-3-methyl-1H-imidazol-3-ium hexafluoridophosphate, C9H15F6N2O2P
  67. Crystal structure of 1-(4-chlorophenyl)-4-(2-furoyl)-3-phenyl-1H-pyrazol-5-ol, C20H13ClN2O3
  68. Crystal structure of dimethyl (R)-2-(3-(1-phenylethyl)thioureido)-[1,1′-biphenyl]-4,4′-dicarboxylate, C25H24N2O4S
  69. The crystal structure of 1-(3-carboxypropyl)-1H-imidazole-3-oxide, C7H10N2O3
  70. Synthesis and crystal structure of dimethyl 4,4′-(propane-1,3-diylbis(oxy))dibenzoate, C19H20O6
  71. Crystal structure of methyl-1-(p-tolyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate, C20H20N2O2
  72. The crystal structure of 1-(1-adamantan-1-yl)ethyl-3-(3-methoxyphenyl)thiourea, C20H28N2OS
  73. The crystal structure of N,N′-carbonylbis(2,6-difluorobenzamide), C15H8F4N2O3
Heruntergeladen am 21.9.2025 von https://www.degruyterbrill.com/document/doi/10.1515/ncrs-2024-0077/html
Button zum nach oben scrollen