59962-93-5

Basic information

• Product Name: 5-phenyl-benzofuran-2-carboxylic acid
• Synonyms: 5-phenyl-benzofuran-2-carboxylic acid
• CAS NO: 59962-93-5
• Molecular Weight: 238.243
• Mol File: 59962-93-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 5-phenyl-benzofuran-2-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 5-phenyl-benzofuran-2-carboxylic acid(59962-93-5)
• EPA Substance Registry System: 5-phenyl-benzofuran-2-carboxylic acid(59962-93-5)

Safety Data

• Hazardous Substances Data: 59962-93-5(Hazardous Substances Data)

Upstream product

• 59962-90-2 ethyl 5-phenylbenzofuran-2-carboxylate 
• 1448818-05-0 3-(2,2-dibromovinyl)biphenyl-4-ol 
• 13939-06-5 molybdenum hexacarbonyl 
• 84102-69-2 5-bromo-benzofuran-2-carboxylic acid ethyl ester 
• 98-80-6 phenylboronic acid 

Downstream Products

• 361456-66-8 (5-phenyl-benzofuran-2-yl)-methanol 
• 59962-94-6 5-phenyl-2,3-dihydro-benzofuran-2-carboxylic acid 

Relevant articles and documents

Tandem Synthesis of 2-Carboxybenzofurans via Sequential Cu-Catalyzed C-O Coupling and Mo(CO)6-Mediated Carbonylation Reactions

A modular tandem synthesis of 2-carboxybenzofurans from 2-gem-dibromovinylphenols has been established based on a sequence of Cu-catalyzed intramolecular C-O coupling and Mo(CO)6-mediated intermolecular carbonylation reactions. This protocol allowed one-step access to a broad variety of functionalized benzofuran-2-carboxylic acids, esters, and amides in good to excellent yields under Pd- and CO gas-free conditions.

Alkoxycarbonylamino benzoic acid or alkoxycarbonylamino tetrazolyl phenyl derivatives as IP antagonists

This invention relates to compounds which are generally IP receptor antagonists and which are represented by Formula I: wherein G1 is selected from the group consisting of a, b1, and b2 and A and G2 are as defin

2,3-Dihydro benzofuran carboxamides

Certain 5-(or 4-)substituted 2,3-dihydro-N-(2-propenyl)-2-benzofurancarboxamides, useful as lipogenesis inhibitors in mammals.