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3-methylphenyl 4-methoxybenzoate is an organic compound with the chemical formula C15H14O3. It is a derivative of benzoic acid, featuring a 3-methylphenyl group attached to the benzoate moiety, and a 4-methoxy substituent on the benzene ring. 3-methylphenyl 4-methoxybenzoate is characterized by its aromatic structure and ester functionality, which contribute to its chemical properties. It is synthesized through the esterification of 3-methylphenol with 4-methoxybenzoic acid and is used in various applications, including the synthesis of pharmaceuticals and as a chemical intermediate in the production of specialty chemicals. The compound's structure and properties make it a valuable component in the field of organic chemistry.

7464-47-3

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7464-47-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7464-47-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7464-47:
(6*7)+(5*4)+(4*6)+(3*4)+(2*4)+(1*7)=113
113 % 10 = 3
So 7464-47-3 is a valid CAS Registry Number.

7464-47-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-methylphenyl) 4-methoxybenzoate

1.2 Other means of identification

Product number -
Other names 4-methoxy-benzoic acid m-tolyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7464-47-3 SDS

7464-47-3Relevant articles and documents

Transition-Metal-Free DMAP-Mediated Aromatic Esterification of Amides with Organoboronic Acids

Guo, Jiarui,Liu, Lantao,Wang, Tao,Wang, Yanqing,Xu, Kai,Zhang, Yuheng

supporting information, p. 3274 - 3277 (2021/06/26)

A new, transition-metal-free, effective method for aromatic esterification of amides with organoboronic acids has been developed. A wide range of benzoate derivatives were obtained with yields ranging from moderate to good. The catalytic reaction shows a broad substrate scope and excellent functional group tolerance. Conceptually, DMAP mediates the reaction and is crucial for this transformation.

K2CO3-promoted formation of aryl esters from primary aryl amides by the acyl-acyl exchange process

Bian, Yongjun,Qu, Xingyu

supporting information, p. 3869 - 3872 (2016/05/24)

A new acyl-acyl exchange reaction has been developed for the formation of aryl esters from primary aryl amides. The reaction could occur under mild reaction conditions with catalytic quantities of K2CO3, and could afford moderate to good yields of the desired products.

Study on the aromatic transesterification reaction catalyzed by phosphotungstic acid

He, Hong-Qiang,Chang, Yu-Wei,Xu, Wei-Ming

supporting information, p. 280 - 282 (2015/06/22)

A practical phosphotungstic acid-catalyzed aromatic transesterification reaction for the preparation of aryl benzoates has been developed. The transesterification method avoids the oxidation of the corresponding phenols to quinone compounds with easy operations, environmentally benign conditions and high yields of the products. It is noteworthy that in this process phosphotungstic acid can be reused and recycled.

The chemoselective preparation of the substituted phenyl benzoates using re-Y zeolite as catalyst

Ding, Yixiang,Wu, Rui,Lin, Qiang

, p. 2149 - 2153 (2007/10/03)

A practical and chemoselective method for the synthesis of substituted phenyl benzoates using rare earth zeolite as catalyst was described, its recycle procedure offers high total yield.

BeCl2 as a new highly selective reagent for dealkylation of aryl-methyl ethers

Sharghi, Hashem,Tamaddon, Fatemeh

, p. 13623 - 13640 (2007/10/03)

An efficient and simple method is introduced for the selective removal of methyl group from poly aryl-methyl ethers, in some important derivatives of benzophenones, xanthones, anthraquinones, aryl esters, benzamides and nitroanisoles with BeCl2.

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