101508-94-5

Basic information

• Product Name: Benzoic acid, 3,5-dihydroxy-, phenylmethyl ester
• CAS NO: 101508-94-5
• Molecular Formula: C14H12O4
• Molecular Weight: 244.247
• Mol File: 101508-94-5.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 3,5-dihydroxy-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 3,5-dihydroxy-, phenylmethyl ester(101508-94-5)
• EPA Substance Registry System: Benzoic acid, 3,5-dihydroxy-, phenylmethyl ester(101508-94-5)

Safety Data

• Hazardous Substances Data: 101508-94-5(Hazardous Substances Data)

Upstream product

• 99-10-5 3,5-Dihydroxybenzoic acid 
• 100-44-7 benzyl chloride 
• 100-51-6 benzyl alcohol 
• 39192-49-9 3,5-diacetoxybenzoyl chloride 
• 100-39-0 benzyl bromide 
• 302836-47-1 3,5-dihydroxy-4-iodobenzoic acid benzyl ester 
• 153444-35-0 benzyl 3,5-diacetoxybenzoate 

Downstream Products

• 153444-36-1 benzyl 3,5-bis(ethoxycarbonylmethoxy)benzoate 
• 957473-22-2 C₂₈H₁₆Cl₂N₆O₇ 
• 153444-40-7 [3-Ethoxycarbonylmethoxy-5-(1,4,10,13-tetraoxa-7,16-diaza-cyclooctadecane-7-carbonyl)-phenoxy]-acetic acid ethyl ester 
• 141810-53-9 16-(3,5-Bis-carboxymethoxy-benzoyl)-1,4,10,13-tetraoxa-7,16-diaza-cyclooctadecane-7-carboxylic acid benzyl ester 
• 141810-49-3 16-(3,5-Bis-ethoxycarbonylmethoxy-benzoyl)-1,4,10,13-tetraoxa-7,16-diaza-cyclooctadecane-7-carboxylic acid benzyl ester 
• 153444-37-2 3,5-bis(ethoxycarbonylmethoxy)benzoic acid 
• 153444-38-3 3,5-bis(ethoxycarbonylmethoxy)benzoyl chloride 
• 945011-02-9 C₃₄H₂₀N₆O₈Cl₂ 
• 1064442-02-9 3-(2-(tert-butoxy)-2-oxoethoxy)-5-isopropoxybenzoic acid 
• 1391999-66-8 benzyl 3-(2-(tert-butoxy)-2-oxoethoxy)-5-isopropoxybenzoate 
• 1391999-78-2 tert-butyl 3-(3-(3-(but-3-en-1-yl)-3-(3-(2-(tert-butoxy)-2-oxoethoxy)-5-isopropoxybenzoyl)ureido)-4-isopropoxyphenyl)propanoate 
• 1391999-79-3 3-(3-(3-allyl-3-(3-(carboxymethoxy)-5-isopropoxybenzoyl)ureido)-4-isopropoxyphenyl)propanoic acid 
• 1391999-77-1 tert-butyl 3-(3-(3-allyl-3-(3-(2-(tert-butoxy)-2-oxoethoxy)-5-isopropoxybenzoyl)ureido)-4-isopropoxyphenyl)propanoate 

Relevant articles and documents

A simple and effective method for chemoselective esterification of phenolic acids

A new method for efficient and chemoselective esterification of phenolic acids in KHCO3/alkyl halide/DMF reaction system is described, by which a series of phenoic acid esters were obtained in excellent yields.

Chemoselective esterification of phenolic acids in the presence of sodium bicarbonate in ionic liquids

Chemoselective esterification of phenolic acids with dialkyl sulphates or alkyl halides in the presence of sodium bicarbonate in 1,3-dialkylimidazolium ionic liquids is reported in excellent yields and less reaction time as compared to organic solvents. Copyright Taylor & Francis Group, LLC.

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PROBLEM TO BE SOLVED: To provide a protein aggregation inhibitor capable of inhibiting protein aggregation and preparing a protein solution with a low viscosity. SOLUTION: The protein aggregation inhibitor contains a compound represented by the general formula (1) in the figure. SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT