15720-16-8

Usage

General Description

Benzenemethanol, 4-(bromomethyl)-, acetate is a chemical compound with the molecular formula C10H11BrO2. It is also known by the chemical name p-bromomethylbenzyl acetate. Benzenemethanol, 4-(bromomethyl)-, acetate is frequently used in organic synthesis as a reagent for the preparation of various organic compounds. It is commonly employed in the production of pharmaceuticals, fragrances, and other fine chemicals. Benzenemethanol, 4-(bromomethyl)-, acetate is a versatile and important chemical building block that is used in a wide range of industrial applications. It is important to handle Benzenemethanol, 4-(bromomethyl)-, acetate with caution, as it may pose hazards to human health and the environment if not managed properly.

Upstream product

• 108-24-7 acetic anhydride 
• 71831-21-5 4-(bromomethyl)benzyl alcohol 
• 623-24-5 1,4-bis(bromomethyl)benzene 
• 127-08-2 potassium acetate 
• 2417-72-3 Methyl 4-(bromomethyl)benzoate 
• 99-75-2 4-methyl-benzoic acid methyl ester 
• 127-09-3 sodium acetate 

Downstream Products

• 17268-36-9 Diethyl <4-(acetoxymethyl)benzyl>acetamidomalonate 
• 161957-78-4 4-(3-methylidenepent-4-enyl)benzyl acetate 
• 1312424-03-5 4-[(1-methylimidazoliumhexafluorophospho)methyl]benzyl 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranoside 
• 1312423-95-2 3-[4-(hydroxymethyl)benzyl]-1-methylimidazolium hexafluorophosphate 
• 1312423-93-0 3-[4-(acetoxymethyl)benzyl]-1-methylimidazolium hexafluorophosphate 
• 1020856-23-8 1,3-di[4-(acetoxymethyl)phenyl]propanone 
• 132067-40-4 N-Acetyl (4-diethoxyphosphonomethyl)-DL-phenylalanine 
• 120667-17-6 4-(Phosphonomethyl)-DL-phenylalanine 
• 132067-39-1 N-Acetyl (4-bromomethyl)-DL-phenylalanine methyl ester 
• 132067-38-0 N-Acetyl (4-hydroxymethyl)-DL-phenylalanine methyl ester 
• 15742-86-6 N-Acetyl (4-hydroxymethyl)-DL-phenylalanine 
• 172362-46-8 2-Bromo-malonic acid methyl ester 4-(3-methylene-pent-4-enyl)-benzyl ester 
• 172362-45-7 Malonic acid methyl ester 4-(3-methylene-pent-4-enyl)-benzyl ester 
• 161957-76-2 2-Bromo-malonic acid bis-[4-(3-methylene-pent-4-enyl)-benzyl] ester 

Relevant academic research and scientific papers

Assembly of homolinear α(1→2)-linked nonamannoside on ionic liquid support

An improved method for the synthesis of large and complex oligosaccharides on ionic liquid (IL) support was developed. A strategy to attach the acceptor on IL using a more stable ether linker was used to prevent undesirable decomposition and side products

Ionic liquids as reaction media for esterification of carboxylate sodium salts with alkyl halides

Ionic liquids based on 1,3-dialkylimidazolinium methanesulfonate have been used as effective reusable reaction media in the esterification of several carboxylate sodium salts with different alkyl halides. Products are easily isolated by extraction with ether, and the protocol is mild and green, compared to the existing methods based on toxic solvents. Proper 'design' of the ionic liquid allows us to obtain esters always in quantitative yields.

26. Multiple Adducts of C60 by Tether-Directed Remote Functionalization and Synthesis of Soluble Derivatives of New Carbon Allotropes Cn(60 + 5)

A comprehensive series of multiple adducts of C60 was prepared by tether-directed remote functionalization. When the tether-reactive-group conjugates 2 and 10 were attached to methano[60]fullerenecarboxylic acid = cyclopropafullerene-C60/

Synthesis of 4-phosphono- and of 4-(phosphonomethyl)-dl-phenylalanine, two analogues of O-phosphotyrosine

:4-Phosphono-DL-phenylalanine 1 was synthetized from 4-bromo-DL-phenylalanine or from 4-(bromomethyl)-bromobenzene ; 4-(phosphonomethyl)-DL-phenylalanine 14 was prepared from methyl p-toluate. The interest of these phosphonic analogues arises from their possible interference in the metabolism of O-phosphotyrosine.