Home Crystal structure of 3-methyl-2-oxo-2H-chromen-7-yl propionate, C13H12O4
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Crystal structure of 3-methyl-2-oxo-2H-chromen-7-yl propionate, C13H12O4

  • Bei-Bei Wang , Chuan-Yi Zang EMAIL logo , Ling Zhang and Wei-Na Wu
Published/Copyright: October 25, 2018

Abstract

C13H12O4, triclinic, P1̄ (no. 2), a = 6.141(5) Å, b = 8.108(6) Å, c = 12.234(9) Å, α = 79.257(12)°, β = 76.820(12)°, γ = 74.687(11)°, V = 566.8(7) Å3, Z = 2, Rgt(F) = 0.0515, wRref(F2) = 0.1575, T = 296(2) K.

CCDC no.: 1872401

The asymmetric unit of the title crystal structure is shown in the figure. Tables 1 and 2 contain details on crystal structure and measurement conditions and a list of the atoms including atomic coordinates and displacement parameters.

Table 1:

Data collection and handling.

Crystal:Colourless rod
Size:0.20 × 0.12 × 0.08 mm
Wavelength:Mo Kα radiation (0.71073 Å)
μ:0.10 mm−1
Diffractometer, scan mode:Bruker APEX-II, φ and ω
θmax, completeness:25.0°, 99%
N(hkl)measured, N(hkl)unique, Rint:2893, 1990, 0.011
Criterion for Iobs, N(hkl)gt:Iobs > 2 σ(Iobs), 1556
N(param)refined:154
Programs:SHELX [1], Bruker [2]
Table 2:

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

AtomxyzUiso*/Ueq
O10.2510(3)0.0298(2)0.85649(15)0.0751(6)
O20.0494(3)−0.12022(19)0.79958(13)0.0610(5)
O30.4041(3)0.3615(3)0.29128(15)0.0809(6)
O40.2805(2)0.22045(19)0.45430(12)0.0540(4)
C10.4215(6)−0.2544(4)1.0112(3)0.0959(10)
H1A0.444679−0.3570351.0650200.144*
H1B0.561221−0.2518710.9569540.144*
H1C0.379030−0.1547901.0500980.144*
C20.2340(5)−0.2536(3)0.9515(2)0.0722(7)
H2A0.276733−0.3560840.9139990.087*
H2B0.094638−0.2590541.0070940.087*
C30.1860(4)−0.0993(3)0.86638(18)0.0553(6)
C4−0.0021(4)0.0090(3)0.71067(17)0.0496(5)
C5−0.2322(4)0.0800(3)0.70763(19)0.0565(6)
H5A−0.3457480.0475620.7660090.068*
C6−0.2902(4)0.1988(3)0.6171(2)0.0567(6)
H6A−0.4444860.2462200.6141490.068*
C7−0.1222(3)0.2496(2)0.52984(17)0.0459(5)
C80.1062(3)0.1751(2)0.53752(16)0.0442(5)
C90.1691(4)0.0535(3)0.62614(17)0.0490(5)
H9A0.3229990.0031770.6285610.059*
C10−0.1680(4)0.3680(3)0.43092(19)0.0523(5)
H10A−0.3198840.4169510.4236220.063*
C110.0003(4)0.4105(3)0.34860(18)0.0510(5)
C120.2373(4)0.3343(3)0.35891(18)0.0543(5)
C13−0.0395(5)0.5291(3)0.2426(2)0.0692(7)
H13A0.1056160.5408560.1958910.104*
H13B−0.1215200.4827650.2021910.104*
H13C−0.1282680.6402150.2613310.104*

Source of material

The title compound was synthesized according to the literature method [3]. Crystals suitable for X-ray diffraction analysis were obtained via recrystallization from an ethanol solution.

Experimental details

The structure was solved by direct methods and refined with the SHELX crystallographic software package [1]. The hydrogen atoms were placed at calculated positions and refined as riding atoms with isotropic displacement parameters.

Comment

Coumarin is a simple flavonoid molecule and is a natural constituent of many plants and essential oils. The synthesis of methylcoumarin derivatives dates back to the beginning of the last century [4]. Coumarin derivatives have been proven to function as an anti-coagulants, antibacterial agents, antifungal agents, biological inhibitors, chemotherapeutics and as bio-analytical reagents [5], [6] .

In the title structure, all bond lengths lie in the normal range and excellently fit with those derived from the crystal structure of the parent compound 3-methyl-2H-chromen-2-one [7]. In the crystal, pairs of weak intermolecular C—H⋯O hydrogen bonds link two molecules into a centrosymmetric dimers. The dimers are weakly connected with others via further C—H⋯O hydrogen bonds, forming a chain structure along a.

References

1. Sheldrick, G. M.: A short history of SHELX. Acta Crystallogr. A64 (2008) 112–122.10.1107/S0108767307043930Search in Google Scholar PubMed

2. Bruker. SMART and SAINT. Bruker AXS Inc., Madison, WI, (USA) (2007).Search in Google Scholar

3. Tang, H.-Y.; Gao, Y.; Li, B.; Li, C.-W.; Guo, Y.: Reaction-based colorimetric and ratiometric fluorescent probe for highly selective detection of silver ions. Sens. Actuators B 270 (2018) 562–569.10.1016/j.snb.2018.05.064Search in Google Scholar

4. Thompson, T. J.; Edee, R. H.: Preparation of 6-methylcoumarin and its derivatives. J. Am. Chem. Soc. 47 (1925) 2556–2559.10.1021/ja01687a019Search in Google Scholar

5. Guha, S.; Lohar, S.; Hauli, I.; Mukhopadhyay, S. K.; Das, D.: Vanillin-coumarin hybrid molecule as an efficient fluorescent probe for trace level determination of Hg(II) and its application in cell imaging. Talanta 85 (2011) 1658–1664.10.1016/j.talanta.2011.06.073Search in Google Scholar PubMed

6. Guha, S.; Lohar, S.; Banerjee, A.; Sahana, A.; Hauli, I.; Mukherjee, S. K.; Matalobos, J. S.; Das, D.: Thiophene anchored coumarin derivative as a turn-on fluorescent probe for Cr3: cell imaging and speciation studies. Talanta 91 (2012) 18–25.10.1016/j.talanta.2011.12.014Search in Google Scholar PubMed

7. Fan-Xin, Z.; Xu-Liang, N.; Xin-Chen, S.-g.; Zhong-Ping, Y.; Da-Yong, P.: Crystal structure of 3-methyl-2H-chromen-2-one, C10H8O2. Z. Kristallogr. NCS 231 (2016) 975–976.10.1515/ncrs-2016-0028Search in Google Scholar

Received: 2018-08-01
Accepted: 2018-10-10
Published Online: 2018-10-25
Published in Print: 2019-03-26

©2019 Bei-Bei Wang et al., published by De Gruyter, Berlin/Boston

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

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