14389-87-8

Basic information

• Product Name: benzyl 2-(benzyloxy)benzoate
• Synonyms: benzyl 2-(benzyloxy)benzoate
• CAS NO: 14389-87-8
• Molecular Weight: 318.372
• Mol File: 14389-87-8.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: benzyl 2-(benzyloxy)benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 2-(benzyloxy)benzoate(14389-87-8)
• EPA Substance Registry System: benzyl 2-(benzyloxy)benzoate(14389-87-8)

Safety Data

• Hazardous Substances Data: 14389-87-8(Hazardous Substances Data)

Upstream product

• 7221-40-1 benzyldimethyl-2-hydroxyethyl-ammonium chloride 
• 69-72-7 salicylic acid 
• 100-44-7 benzyl chloride 
• 606-45-1 2-methoxybenzoic acid methyl ester 
• 68-12-2 N,N-dimethyl-formamide 
• 20194-18-7 sodium phenyl-methanolate 
• 100-39-0 benzyl bromide 
• 103-83-3 N,N'-dimethylbenzylamine 
• 119-36-8 methyl salicylate 

Downstream Products

• 118-58-1 benzyl salicylate 
• 1258196-71-2 [2-(benzyloxy)phenyl](2,5-dimethoxyphenyl)methanone 
• 1258196-68-7 [2-(benzyloxy)phenyl](1,4-dimethoxynaphthalen-2-yl)methanone 
• 1258196-72-3 (2-(benzyloxy)phenyl)(2,4,5-trimethoxyphenyl)methanone 
• 6702-58-5 4-methoxy-9H-xanthen-9-one 
• 14389-86-7 2-benzyloxybenzoic acid 
• 142819-91-8 1-(2-benzyloxyphenyl-2-diazopropan-1-one 
• 195813-61-7 3-(2'-hydroxyphenyl)-5-(2-benzyloxyphenyl)pyrazole 
• 164170-38-1 2'-(2-benzyloxybenzoyloxy)acetophenone 
• 893393-33-4 C₁₇H₁₅⁽²⁾HO 
• 100-51-6 benzyl alcohol 
• 71367-02-7 C₁₄H₁₁⁽²⁾HO₂ 

Relevant articles and documents

Facile alkoxyl exchange of 2-methoxybenzoates via nucleophilic aromatic substitution with sodium alkoxides in dimethylformamide

Methyl 2-methoxybenzoate undergoes facile nuclear-methoxyl displacement by treatment with sodium butexide or isopropoxide in dimethylformamide.

GLUCOSAMINE DERIVATIVES AND PHARMACEUTICAL USES THEREOF

There are provided compounds of Formula (A) and pharmaceutically acceptable salts and esters thereof, and pharmaceutical compositions thereof, used for the prevention or treatment in a mammal of joint and bone disorders such as arthritis and osteoporosis.

Highly efficient and green esterification of carboxylic acids in deep eutectic solvents without any other additives

A protocol that carboxylic acids esterifies with the quaternary ammonium salt of deep eutectic solvent (DES) is presented, which opens a new access to ester using DES as alkylating agent, solvent, and catalyst. The reaction runs smoothly in DES without any other additives. Substituted cinnamic acids, aromatic acids, and aliphatic acids can be esterified in moderate to good yields. The advantages of this reaction include excellent functional group compatibility and simple reaction procedure.