154629-81-9

Basic information

• Product Name: methyl 4-phenylbenzo[b]thiophene-2-carboxylate
• Synonyms: methyl 4-phenylbenzo[b]thiophene-2-carboxylate
• CAS NO: 154629-81-9
• Molecular Weight: 268.336
• Mol File: 154629-81-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: methyl 4-phenylbenzo[b]thiophene-2-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 4-phenylbenzo[b]thiophene-2-carboxylate(154629-81-9)
• EPA Substance Registry System: methyl 4-phenylbenzo[b]thiophene-2-carboxylate(154629-81-9)

Safety Data

• Hazardous Substances Data: 154629-81-9(Hazardous Substances Data)

Upstream product

• 149732-36-5 4-iodobenzo[b]thiophene-2-carboxamidine hydrochloride 
• 1080-43-9 dimethyldiphenyltin 
• 146137-85-1 methyl 4-iodobenzo[b]thiophene-2-carboxylate 
• 360575-28-6 2-bromo-6-fluorobenzaldehyde 
• 1073-06-9 3-fluorobromobenzene 
• 98-80-6 phenylboronic acid 
• 360575-29-7 methyl 4-bromobenzo[b]thiophene-2-carboxylate 

Relevant articles and documents

METHOD FOR PROMOTING PLANT GROWTH

The present invention provides a method for promoting plant growth, which comprises treating a plant with a compound represented by the following Formula (1): provided that a method for promoting plant growth which comprises treating plants with a compound corresponding to any one of the following (1) to (8) is excluded: (1) Methyl 4-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, (2) Methyl 5-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, (3) Methyl 6-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, (4) Methyl 7-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, (5) Ethyl 4-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, (6) Ethyl 5-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, (7) Ethyl 6-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, and (8) Ethyl 7-(trifluoromethyl)benzo[b]thiophene-2-carboxylate.

4-Substituted (benzo[b]thiophene-2-carbonyl)guanidines as novel Na +/H+ exchanger isoform-1 (NHE-1) inhibitors

A series of 4-substituted (benzo[b]thiophene-2-carbonyl)guanidines was synthesized and evaluated for the NHE-1 inhibitory activity and cardioprotective efficacy both in vitro and in vivo. Several analogs exhibited a strong inhibition on NHE-1, and which was generally well correlated with their cardioprotective efficacy. Especially the 4-nitro 20 and cyano 50 compounds excellently improved the cardiac function and reduced infarct size against ischemia/reperfusion injury.