143211-21-6

Basic information

• Product Name: 2-[(2-methylphenoxy)methyl]benzoyl chloride
• Synonyms: 2-[(2-Methylphenoxy)methyl]benzoyl chloride; benzoyl chloride, 2-[(2-methylphenoxy)methyl]-
• CAS NO: 143211-21-6
• Molecular Formula: C₁₅H₁₃ClO₂
• Molecular Weight: 260.7155
• EINECS: 604-339-0
• Mol File: 143211-21-6.mol

Chemical Properties

• Boiling Point: 385.4°C at 760 mmHg
• Flash Point: 141.6°C
• Density: 1.202g/cm³
• Vapor Pressure: 3.82E-06mmHg at 25°C
• Refractive Index: 1.583
• CAS DataBase Reference: 2-[(2-methylphenoxy)methyl]benzoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(2-methylphenoxy)methyl]benzoyl chloride(143211-21-6)
• EPA Substance Registry System: 2-[(2-methylphenoxy)methyl]benzoyl chloride(143211-21-6)

Safety Data

• Hazardous Substances Data: 143211-21-6(Hazardous Substances Data)

Upstream product

• 95-48-7 ortho-cresol 
• 87-41-2 2-benzofuran-1(3H)-one 
• 108475-90-7 2-[(2-methylphenoxy)methyl]benzoic acid 

Downstream Products

• 1397689-10-9 4-(3-carboxamido-4-hydroxyphenyl)-2-[(2-methylphenoxymethyl)phenyl]-[1,3]-thiazole 
• 1397689-14-3 4-(5-chloro-2-sulfonamidothien-3-yl)-2-[(2-methylphenoxymethyl)phenyl]-[1,3]-thiazole 
• 1397689-18-7 4-(3-bromophenyl)-2-[(2-methylphenoxymethyl)phenyl]-[1,3]-thiazole 
• 1397689-22-3 4-(4-nitrophenyl)-2-[(2-methylphenoxymethyl)phenyl]-[1,3]-thiazole 
• 1397689-26-7 4-chloromethyl-2-[2-(2-methylphenoxymethyl)phenyl]-[1,3]-thiazole 
• 1397689-29-0 4-[4-(diphenylmethyl)piperzin-1-yl]methyl-2-[2-(2-methylphenoxymethyl)phenyl]-[1,3]-thiazole 
• 1397689-33-6 4-[4-({4-chlorophenyl}{phenyl}methyl)piperzin-1-yl]methyl-2-[2-(2-methylphenoxymethyl)phenyl]-[1,3]-thiazole 
• 1397689-37-0 4-(4-chlorophenoxy)methyl-2-[2-(2-methylphenoxymethyl)phenyl]-[1,3]-thiazole 
• 1483100-01-1 C₁₅H₁₅NO₂ 
• 143211-11-4 2-[(2-methylphenoxy)methyl]benzoyl cyanide 
• 143358-86-5 2-o-tolyloxymethylbenzoic acid methyl ester 
• 143211-10-3 2-oxo-2-(((o-tolyl)oxymethyl)phenyl)acetic acid methyl ester 
• 108475-90-7 2-[(2-methylphenoxy)methyl]benzoic acid 
• 143390-89-0 methyl (E)-2-methoxyimino-2-[2-(o-tolyloxymethyl)phenyl]acetate 

Relevant articles and documents

Green synthetic method of kresoxim-methyl

The invention belongs to the technical field of fine chemical engineering, and particularly relates to a green synthetic method of kresoxim-methyl. The method comprises the following steps: carrying out nitrous nitrification by using 2-methylbenzyl cyanide as an initial raw material, carrying out methylation, carrying out hydrolytic methylation or hydrolytic esterification, carrying out bromination and carrying out an etherification reaction to obtain the high-content kresoxim-methyl. The method provided by the invention has a short reaction period, a high conversion rate, and excellent product quality, changes the defect that high-concentration hydrochloric acid gas is used for preparation in a traditional process, and has the advantages of simple operation steps, simple equipment, low energy consumption, a short period, high productivity and environmental protection.

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A series of 2,4-disubstituted-[1,3]-thiazoles (4a-p and 6a-l) was synthesized from 2-(aryloxymethyl)benzoic acids (1a-d) through a multistep reaction sequence in good yield. The structures of the new compounds were established on the basis of their elemen

AN IMPROVED PROCESS FOR THE SYNTHESIS OF STROBILURIN FUNGICIDES VIZ TRIFLOXYSTROBIN AND KRESOXIM-METHYL

The present invention relates to an improved process for the synthesis of E-isomer of compound of formula (5). It further relates to the conversion of formula (5), wherein R is H, to Intermediate (I) and subsequently to substantially pure Trifloxystrobin, compound of formula (I) in good yield.

Preparation of E-oxime ethers of phenylglyoxylic esters

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