68257-90-9

Basic information

• Product Name: 5-(BROMOACETYL)THIOPHENE-2-CARBOXAMIDE
• Synonyms: 5-(BROMOACETYL)THIOPHENE-2-CARBOXAMIDE;2-THIOPHENECARBOXAMIDE, 5-(BROMOACETYL);5-(2-BroMoacetyl)thiophene-2-carboxaMide
• CAS NO: 68257-90-9
• Molecular Formula: C7H6BrNO2S
• Molecular Weight: 248.09704
• Mol File: 68257-90-9.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-(BROMOACETYL)THIOPHENE-2-CARBOXAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(BROMOACETYL)THIOPHENE-2-CARBOXAMIDE(68257-90-9)
• EPA Substance Registry System: 5-(BROMOACETYL)THIOPHENE-2-CARBOXAMIDE(68257-90-9)

Safety Data

• Hazardous Substances Data: 68257-90-9(Hazardous Substances Data)

Usage

Uses

5-(Bromoacetyl)thiophene-2-carboxamide is used for β-adrenergic blocking actions.

Upstream product

• 4101-81-9 methyl 5-acetyl-2-thiophenecarboxylate 
• 89692-69-3 5-acetyl-thiophene-2-carbonyl chloride 
• 4066-41-5 5-acetylthiophene-2-carboxylic acid 
• 114774-09-3 5-(α-methoxyimino)ethyl-2-thiophenecarboxylic acid 
• 114774-08-2 5-acetyl-2-(α-methoxyimino)ethylthiophene 
• 114773-97-6 2-(α-methoxyimino)ethylthiophene 
• 88-15-3 2-Acetylthiophene 
• 68257-89-6 5-acetylthiophene-2-carboxamide 

Downstream Products

• 52560-89-1 5-(2-mercapto-1,3-thiazol-4-yl)-2-thiophene carboxamide 
• 101540-26-5 arotinolol hydrochloride 

Relevant articles and documents

Preparation method of arotinolol hydrochloride

The invention provides a preparation method of arotinolol hydrochloride, which comprises the following steps of: reacting a compound shown as a structural formula VIII with absolute methanol in the presence of concentrated sulfuric acid to obtain a compou

Heterocyclic compounds, processes for their preparation and their use

Thiophene carboxamides are described of general formula I STR1 in which the amide function is in the 2- or 3-position on the thiophene ring, R1 to R5 inclusive are hydrogen atoms or lower alkyl groups, X is --CH2 --, --O-- or --NR6 -- where R6 is hydrogen or a lower alkyl group, n is a number from 0 to 3 and Ar is an optionally substituted phenyl group and their physiologically acceptable salts. The compounds have been found to lower blood pressure in animals and to exhibit a blocking action at β-adrenoreceptors and their use is indicated for the treatment of cardiovascular disorders such as hypertension and angina. Some of the compounds also exhibit a blocking action on α-adrenoreceptors and their use is indicated for the treatment of hypertention.