1917-16-4

Basic information

• Product Name: 5-BENZYL-2-FUROIC ACID
• Synonyms: 5-BENZYL-2-FUROIC ACID;5-(phenylmethyl)-2-furancarboxylic acid;5-(phenylmethyl)furan-2-carboxylic acid;5-Benzylfuran-2-carboxylic acid
• CAS NO: 1917-16-4
• Molecular Formula: C₁₂H₁₀O₃
• Molecular Weight: 202.21
• Mol File: 1917-16-4.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 359.7°Cat760mmHg
• Flash Point: 171.4°C
• Appearance: /
• Density: 1.231g/cm³
• Vapor Pressure: 8.4E-06mmHg at 25°C
• Refractive Index: 1.582
• CAS DataBase Reference: 5-BENZYL-2-FUROIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 5-BENZYL-2-FUROIC ACID(1917-16-4)
• EPA Substance Registry System: 5-BENZYL-2-FUROIC ACID(1917-16-4)

Safety Data

• Hazardous Substances Data: 1917-16-4(Hazardous Substances Data)

Usage

General Description

5-Benzyl-2-furoic acid is a chemical compound with the formula C14H12O3. It is a furoic acid derivative with a benzyl group attached at the 5-position of the furan ring. 5-BENZYL-2-FUROIC ACID has potential applications in medicinal chemistry, particularly in the development of pharmaceuticals and agrochemicals. It may also have use in the synthesis of other organic compounds. Its properties and reactivity make it a valuable building block for the creation of new molecules with specific functional groups and biological activities. Overall, 5-benzyl-2-furoic acid is a versatile chemical with promising potential in various fields of science and industry.

InChI:InChI=1/C12H10O3/c13-12(14)11-7-6-10(15-11)8-9-4-2-1-3-5-9/h1-7H,8H2,(H,13,14)

Upstream product

• 58972-21-7 5-Methoxycarbonyl-furan-2-yl phenyl ketone 
• 35897-51-9 5-benzoyl-furan-2-carboxylic acid 
• 71088-89-6 5-furan-2-carboxylic acid 
• 2144-37-8 methyl 5-(chloromethyl)-2-furoate 
• 100-44-7 benzyl chloride 
• 611-13-2 2-furoic acid methyl ester 
• 34885-96-6 methyl 5-benzyl-2-furancarboxylate 

Relevant articles and documents

Regioselective and Stereoselective Pd-Catalyzed Intramolecular Arylation of Furans: Access to Spirooxindoles and 5H-Furo[2,3-c]quinolin-4-ones

Herein, we report regio- and stereoselective intramolecular direct arylations of N-(2-bromophenyl)-2-furancarboxamides 1 to produce spirooxindoles 2 and 5H-furo[2,3-c]quinolin-4-ones 3 under different reaction conditions. Specifically, in the presence of

NOVEL PROCESSES FOR THE PREPARATION OF SUBSTITUTED PROPENONE DERIVATIVES

The present invention provides industrial and commercial processes for the preparation of 2-acyl-5-benzylfuran derivatives, 1,2,4-triazole-3-carboxylic acid ester derivatives and propenone derivatives having anti-HIV activities and usuful crystals thereof. wherein R1, R2 and R4 each is independently hydrogen or the like; A is CR6 or N; R6 is hydrogen or the like; Q is a protecting group; and L is a leaving group.