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Literature DB >> 23795042

(2E)-1-(5-Bromothiophen-2-yl)-3-(4-chloro-phen-yl)prop-2-en-1-one.

H D Kavitha¹, K R Roopashree, Suresh B Vepuri, H C Devarajegowda, Venkatesh B Devaru.

Abstract

In the title compound, C13H8BrClOS, the thio-phene and phenyl rings are inclined by 40.69 (11)° to each other. The crystal structure is characterized by C-H⋯π inter-actions, which link the mol-ecules into broad layers parallel to (100). Short Br⋯Cl contacts [3.698 (1) Å] link these layers along [100].

Entities: Chemical Disease Gene

Year: 2013 PMID： 23795042 PMCID： PMC3684940 DOI： 10.1107/S1600536813012063

Source DB: PubMed Journal: Acta Crystallogr Sect E Struct Rep Online ISSN： 1600-5368

5 in total

1. In vitro antifungal evaluation and structure-activity relationships of a new series of chalcone derivatives and synthetic analogues, with inhibitory properties against polymers of the fungal cell wall.

Authors: S N López; M V Castelli; S A Zacchino; J N Domínguez; G Lobo; J Charris-Charris; J C Cortés; J C Ribas; C Devia; A M Rodríguez; R D Enriz
Journal: Bioorg Med Chem Date: 2001-08 Impact factor: 3.641

1 in total

1. The crystal structures of six (2E)-3-aryl-1-(5-halogeno-thio-phen-2-yl)prop-2-en-1-ones.

Authors: Vasant S Naik; Hemmige S Yathirajan; Jerry P Jasinski; Victoria A Smolenski; Christopher Glidewell
Journal: Acta Crystallogr E Crystallogr Commun Date: 2015-08-26

1 in total

(2E)-1-(5-Bromothiophen-2-yl)-3-(4-chloro-phen-yl)prop-2-en-1-one.

1. In vitro antifungal evaluation and structure-activity relationships of a new series of chalcone derivatives and synthetic analogues, with inhibitory properties against polymers of the fungal cell wall.

2. Structure-activity relationship studies on chalcone derivatives. the potent inhibition of chemical mediators release.

3. Structure-activity relationships of antileishmanial and antimalarial chalcones.

4. A short history of SHELX.

5. (2E)-3-(2-Bromo-phen-yl)-1-(5-bromo-thio-phen-2-yl)prop-2-en-1-one.

1. The crystal structures of six (2E)-3-aryl-1-(5-halogeno-thio-phen-2-yl)prop-2-en-1-ones.