S-Phenyl 4-methoxybenzothioate

被引:2
作者
El-Azab, Adel S. [1 ,2 ]
Abdel-Aziz, Alaa A. -M. [1 ,3 ]
El-Subbagh, Hussein I. [4 ]
Chantrapromma, Suchada [5 ]
Fun, Hoong-Kun [6 ]
机构
[1] King Saud Univ, Coll Pharm, Dept Pharmaceut Chem, Riyadh 11451, Saudi Arabia
[2] Al Azhar Univ, Fac Pharm, Dept Organ Chem, Cairo 11884, Egypt
[3] Univ Mansoura, Fac Pharm, Dept Med Chem, Mansoura 35516, Egypt
[4] Future Univ, Fac Pharmaceut Sci & Pharmaceut Ind, Dept Pharmaceut Chem, Cairo 12311, Egypt
[5] Prince Songkla Univ, Fac Sci, Dept Chem, Crystal Mat Res Unit, Hat Yai 90112, Thailand
[6] Univ Sains Malaysia, Sch Phys, X Ray Crystallog Unit, Usm 11800, Penang, Malaysia
来源
ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS | 2012年 / 68卷
关键词
D O I
10.1107/S1600536812005454
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
In the molecule of the title thioester, C14H12O2S, the dihedral angle between the phenyl and benzene rings is 71.8 (3)degrees. The methoxy group is essentially coplanar with the benezene ring to which it is bonded, with an r.m.s. deviation of 0.0065 (5) A degrees for the non-H atoms involved. In the crystal, weak C-H center dot center dot center dot pi interactions are present.
引用
收藏
页码:O1074 / +
页数:7
相关论文
共 17 条
  • [1] Agapiou K., Krische M.J., Org. Lett., 5, pp. 1737-1740, (2003)
  • [2] Allen F.H., Kennard O., Watson D.G., Brammer L., Orpen A.G., Taylor R., J. Chem. Soc. Perkin Trans., 2, (1987)
  • [3] Barbero M., Degani I., Dughera S., Fochi R., Synthesis, pp. 1225-1230, (2003)
  • [4] APEX2, SAINT and SADABS., (2009)
  • [5] Choi J., Imai E., Mihara M., Oderaotoshi Y., Minakata S., Komatsu M., J. Org. Chem., 68, pp. 6164-6171, (2003)
  • [6] El-Azab A.S., Abdel-Aziz A.A.-M., Phosphorus Sulfur Silicon Relat. Elem., (2012)
  • [7] Flack H.D., Acta Cryst., A39, pp. 876-881, (1983)
  • [8] Horst B., Feringa B.L., Minnaard A.J., Org. Lett., 9, pp. 3013-3015, (2007)
  • [9] Howell G.P., Fletcher S.P., Geurts K., Horst B., Feringa B.L., J. Am. Chem. Soc., 128, pp. 14977-14985, (2006)
  • [10] Jew S., Park B., Lim D., Kim M.G., Chung I.K., Kim J.H., Hong C.I., Kim J., Park H., Lee J., Park H., Bioorg. Med. Chem. Lett., 13, pp. 609-612, (2003)