4-Methyl-2-oxo-2,3-dihydro-1-benzopyran-7-yl benzenesulfonate

被引:2
作者
Yang, Shu-Ping [1 ]
Wang, Da-Qi [2 ]
Han, Li-Jun [3 ]
Liu, Yu-Fen [1 ]
机构
[1] Huaihai Inst Technol, Sch Chem Engn, Lianyungang 222005, Peoples R China
[2] Liaocheng Univ, Coll Chem & Chem Engn, Liaocheng 252059, Shandong, Peoples R China
[3] Huaihai Inst Technol, Sch Math & Sci, Lianyungang 222005, Peoples R China
来源
ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE | 2008年 / 64卷
关键词
D O I
10.1107/S1600536808032005
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
The title compound, C(16)H(12)O(5)S, is a derivative of coumarin. The dihedral angle between the coumarin ring system and the phenyl ring is 65.9 (1)degrees. In the crystal structure, molecules are linked by weak C-H center dot center dot center dot O hydrogen bonding to form molecular ribbons.
引用
收藏
页码:O2088 / U1653
页数:10
相关论文
共 10 条
[1]   Esters and amides of 6-(chloromethyl)-2-oxo-2H-1-benzopyran-3-carboxylic acid as inhibitors of alpha-chymotrypsin: Significance of the ''aromatic'' nature of the novel ester-type coumarin for strong inhibitory activity [J].
Pochet, L ;
Doucet, C ;
Schynts, M ;
Thierry, N ;
Boggetto, N ;
Pirotte, B ;
Jiang, KY ;
Masereel, B ;
deTullio, P ;
Delarge, J ;
ReboudRavaux, M .
JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (13) :2579-2585
[2]   SYNTHESIS OF COUMARINS AS SUBTYPE-SELECTIVE INHIBITORS OF MONOAMINE-OXIDASE [J].
RENDENBACHMULLER, B ;
SCHLECKER, R ;
TRAUT, M ;
WEIFENBACH, H .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1994, 4 (10) :1195-1198
[3]   A non-radioactive microtitre plate reverse transcriptase (RT) assay, based on immobilized template, for screening of RT activity inhibitors and evaluation of their mode of action [J].
Shao, X ;
Ekstrand, DHL ;
Bhikhabhai, R ;
Kallander, CFR ;
Gronowitz, JS .
ANTIVIRAL CHEMISTRY & CHEMOTHERAPY, 1997, 8 (02) :149-159
[4]  
Sheldrick G.M., 1996, SADABS VERSION 2008
[5]   A short history of SHELX [J].
Sheldrick, George M. .
ACTA CRYSTALLOGRAPHICA A-FOUNDATION AND ADVANCES, 2008, 64 :112-122
[6]  
*SIEM AN XR INSTR, 1996, SMART SAINT
[7]   Synthesis and antibacterial activity of a novel series of potent DNA gyrase inhibitors. Pyrazole derivatives [J].
Tanitame, A ;
Oyamada, Y ;
Ofuji, K ;
Fujimoto, M ;
Iwai, N ;
Hiyama, Y ;
Suzuki, K ;
Ito, H ;
Terauchi, H ;
Kawasaki, M ;
Nagai, K ;
Wachi, M ;
Yamagishi, J .
JOURNAL OF MEDICINAL CHEMISTRY, 2004, 47 (14) :3693-3696
[8]   Anti-AIDS agents.: 42.: Synthesis and anti-HIV activity of disubstituted (3′R,4′R)-3′,4′-di-O-(S)-camphanoyl-(+)-cis-khellactone analogues [J].
Xie, L ;
Takeuchi, Y ;
Cosentino, LM ;
McPhail, AT ;
Lee, KH .
JOURNAL OF MEDICINAL CHEMISTRY, 2001, 44 (05) :664-671
[9]   4-Methyl-7-phenylsulfonamido-2H-1-benzo-pyran-2-one [J].
Yang, Shu-Ping ;
Han, Li-Jun ;
Wang, Da-Qi .
ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2007, 63 :O135-O137
[10]   (E)-7-[(3-chlorocinnamoyl)oxy]-4-methylcoumarin [J].
Yang, Shu-Ping ;
Han, Li-Jun ;
Wang, Da-Qi ;
Xia, Hai-Tao .
ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2006, 62 :O4350-O4352