CAS 22876-19-3
:5-Chloro-2-mercaptobenzoxazole
- 2(3H)-Benzoxazolethione, 5-chloro-
- 2-Benzoxazolethiol, 5-chloro-
- 2-Benzoxazolinethione, 5-chloro-
- 2-Mercapto-5-chlorobenzoxazole
- 5-Chloro-1,3-benzoxazole-2-thiol
- 5-Chloro-2(3H)-benzoxazolethione
- 5-Chloro-2-benzoxazolethiol
- 5-Chloro-2-benzoxazolinethione
- 5-Chloro-2-mercapto-benzoxazol
- 5-Chloro-2-mercaptobenzoxazole
- 5-Chloro-2-thioxobenzoxazoline
- 5-Chloro-benzooxazole-2-thiol
- 5-chlorobenzo[d]oxazole-2(3H)-thione
- See more synonyms
5-Chlorobenzooxazole-2-Thiol
CAS:Formula:C7H4ClNOSPurity:98%Color and Shape:SolidMolecular weight:185.63085-Chloro-1,3-benzoxazole-2-thiol
CAS:5-Chloro-1,3-benzoxazole-2-thiolPurity:≥95%Molecular weight:185.63g/mol5-Chloro-2-mercaptobenzoxazole
CAS:5-Chloro-2-mercaptobenzoxazole is an antibacterial agent that binds to the G protein-coupled receptor subtype. It has been shown to reduce inflammatory pain and increase gastrointestinal motility. 5-Chloro-2-mercaptobenzoxazole interacts with a number of other molecules, such as proteins, DNA, RNA and lipids. This drug has been shown to have cytotoxic effects against human cancer cells in vitro. The molecular structure of 5-chloro-2 mercaptobenzoxazole is a heterocycle which can be synthesized.
5-Chloro-2 mercaptobenzoxazole binds to the G protein coupled receptor subtype and inhibits inflammatory pain by blocking substance P from binding to its receptor. It also increases gastrointestinal motility by interacting with receptors found in the smooth muscle cells of the intestines. 5-Chloro-2 mercaptobenzoxFormula:C7H4CINSOPurity:Min. 95%Color and Shape:White To Off-White SolidMolecular weight:185.63 g/mol5-Chlorobenzo[d]oxazole-2-thiol
CAS:Formula:C7H4ClNOSPurity:95.0%Color and Shape:SolidMolecular weight:185.63




