54373-50-1

Basic information

• Product Name: Carbonic acid, 4-(chloromethyl)-3,5-dimethylphenyl ethyl ester
• Synonyms: carbonic acid ethyl ester-(4-chloromethyl-3,5-dimethyl-phenyl ester);4-Chloromethyl-3,5-dimethylphenyl ethyl carbonate;o-carboethoxy-3,5-dimythyl-4-(chloramethyl)phenol;O-carbethoxy-3,5-dimethyl-4-chloromethylphenol;4-Chlormethyl-3,5-dimethylphenyl-aethylcarbonat;Kohlensaeure-aethylester-(4-chlormethyl-3,5-dimethyl-phenylester);Aethyl-(3.5-dimethyl-4-chlormethyl-phenyl)-carbonat;Carbonic acid,4-(chloromethyl)-3,5-dimethylphenyl ethyl ester
• CAS NO: 54373-50-1
• Molecular Formula: C12H15ClO3
• Molecular Weight: 242.702
• Mol File: 54373-50-1.mol

Chemical Properties

• CAS DataBase Reference: Carbonic acid, 4-(chloromethyl)-3,5-dimethylphenyl ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbonic acid, 4-(chloromethyl)-3,5-dimethylphenyl ethyl ester(54373-50-1)
• EPA Substance Registry System: Carbonic acid, 4-(chloromethyl)-3,5-dimethylphenyl ethyl ester(54373-50-1)

Safety Data

• Hazardous Substances Data: 54373-50-1(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 26177-58-2 3,5-Dimethylphenyl ethyl carbonate 
• 107-30-2 chloromethyl methyl ether 
• 108-68-9 3,5-Dimethylphenol 
• 109-87-5 Dimethoxymethane 

Downstream Products

• 527-54-8 3,4,5-trimethylphenol 
• 33901-24-5 4-Cyanomethyl-3,5-dimethylphenol 
• 194857-83-5 2-(4-hydroxy-2,6-dimethylbenzyl)-2-methylmalonic acid diethyl ester 
• 254102-29-9 (R,S)-2-cyano-3-(4-hydroxy-2',6'-dimethylphenyl)-propanoic acid ethyl ester 
• 254102-30-2 (R,S)-2-cyano-3-(4-hydroxy-2',6'-dimethylphenyl)-propanoic acid 
• 194857-85-7 3-(4-hydroxy-2,6-dimethylbenzyl)-2-methylpropionic acid 
• 194857-86-8 (Des-NH2-αMe-L/D-Dmt)-Tic-OtBu 
• 1185756-57-3 4-iodomethyl-3,5-dimethylphenyl ethyl carbonate 
• 123715-02-6 H-Dmt 
• 90920-20-0 4-Trichlormethyl-3,4,5-trimethyl-cyclohexadien-(2,5)-on-⁽¹⁾ 
• 21354-74-5 4-Hydroxy-2,6-dimethylphenylacetic acid 

Relevant articles and documents

An efficient and convenient chloromethylation of some aromatic compounds catalyzed by zinc iodide

Treatment of a series of aromatic hydrocarbons and O-carbethoxy phenol substrates with a mixture of chlorosulfonic acid and dimethoxymethane in CH2Cl2 catalyzed by zinc iodide affords the corresponding chloromethyl derivatives in good to excellent yields.

A practical and convenient Blanc-type chloromethylation catalyzed by zinc chloride under solvent-free conditions

Chloromethylation of various aromatic hydrocarbons and substituted phenolic derivatives with dimethoxymethane and chlorosulfonic acid was carried out in the presence of 10 mol% of ZnCl2 in a mild and efficient manner under solvent-free conditions. In addition, 2,6-dimethyltyrosine was synthesized in high yield via this protocol.

N, N - diethyl - carboxylic acid 4 - halomethyl - 3, 5 - dimethyl - phenol ester compound and its preparation method

The invention relates to an N,N-diethyl-formic acid 4-halogenate methyl-3,5-dimethyl-phenol ester compound and a preparing method thereof. The compound is used for synthesis of dimethyl tyrosine. The compound is more effective than compounds involved in t

Syntheses of 4-Hydroxy-2,6-dimethylbenzoic Acid and Its Higher Homologues

Syntheses of 4-hydroxy-2,6-dimethylbenzoic acid (2a) and its higher homologues, viz 4-hydroxy-2,6-dimethylphenylacetic acid (2b), 3-(4-hydroxy-2,6-dimethylphenyl)propanoic acid (2c) and 4-(4-hydroxy-2,6-dimethylphenyl)butanoic acid (2d) are described.