339094-04-1

Basic information

• Product Name: Benzoic acid, 3-bromo-, phenylmethyl ester
• CAS NO: 339094-04-1
• Molecular Formula: C14H11BrO2
• Molecular Weight: 291.144
• Mol File: 339094-04-1.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 3-bromo-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 3-bromo-, phenylmethyl ester(339094-04-1)
• EPA Substance Registry System: Benzoic acid, 3-bromo-, phenylmethyl ester(339094-04-1)

Safety Data

• Hazardous Substances Data: 339094-04-1(Hazardous Substances Data)

Upstream product

• 585-76-2 m-bromobenzoic acid 
• 108-88-3 toluene 
• 1711-09-7 3-bromobenzoyl chloride 
• 100-51-6 benzyl alcohol 
• 3132-99-8 m-bromobenzoic aldehyde 
• 100-39-0 benzyl bromide 

Downstream Products

• 1421009-26-8 C₂₃H₂₀O₆ 
• 585-76-2 m-bromobenzoic acid 
• 392743-58-7 3-{bis[4-(phenylsulfonyl)phenoxy]phosphinyl}benzoic acid benzyl ester 

Relevant articles and documents

COMPOUNDS AND THERAPEUTIC USES THEREOF

The invention relates to novel compounds with the ability to link an immune response to a defined therapeutic target, to the use of said compounds in treating cancer and infectious diseases, to compositions containing said compounds, processes for their preparation and to novel intermediates used in said process.

COMPOUNDS AND THERAPEUTIC USES THEREOF

The invention relates to novel compounds with the ability to link an immune response to a pathogen, to the use of said compounds in a disease or disorder mediated and/or caused by an infective agent, to compositions containing said compounds, processes for their preparation and to novel intermediates used in said process.

Reusable ionic liquid-catalyzed oxidative esterification of carboxylic acids with benzylic hydrocarbons via benzylic Csp3-H bond activation under metal-free conditions

A metal-free protocol for the direct oxidative esterification of the Csp3-H bond in benzylic hydrocarbons with carboxylic acids using heterocyclic ionic liquid as catalyst has been reported. The catalyst 1-butylpyridinium iodide could be easily recycled and reused for at least four cycles without obvious loss of catalytic activity.