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4-methylphenyl 3-chlorobenzoate is an organic compound with the chemical formula C14H11ClO2. It is a derivative of benzoic acid, featuring a 4-methylphenyl group attached to the benzene ring and a 3-chloro substituent on the adjacent benzene ring. 4-methylphenyl 3-chlorobenzoate is characterized by its aromatic structure and the presence of a chlorine atom, which imparts unique chemical properties. It is used in various applications, including the synthesis of pharmaceuticals and other organic compounds, due to its reactivity and the ability to form different types of chemical bonds. The compound's molecular weight is 246.68 g/mol, and it is typically obtained as a white crystalline solid.

6280-49-5

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6280-49-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6280-49-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6280-49:
(6*6)+(5*2)+(4*8)+(3*0)+(2*4)+(1*9)=95
95 % 10 = 5
So 6280-49-5 is a valid CAS Registry Number.

6280-49-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methylphenyl) 3-chlorobenzoate

1.2 Other means of identification

Product number -
Other names 3-Chlor-benzoesaeure-p-tolylester

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:6280-49-5 SDS

6280-49-5Upstream product

6280-49-5Relevant academic research and scientific papers

Convenient synthesis of benziodazolone: New reagents for direct esterification of alcohols and amidation of amines

Postnikov, Pavel S.,Rohde, Gregory T.,Saito, Akio,Shea, Michael T.,Vlasenko, Yulia A.,Yoshimura, Akira,Yusubov, Mekhman S.,Zhdankin, Viktor V.

, (2021/12/17)

Hypervalent iodine heterocycles represent one of the important classes of hypervalent iodine reagents with many applications in organic synthesis. This paper reports a simple and convenient synthesis of benziodazolones by the reaction of readily available iodobenzamides with m-chloroperoxybenzoic acid in acetonitrile at room temperature. The structure of one of these new iodine heterocycles was confirmed by X-ray analysis. In combination with PPh3 and pyridine, these benziodazolones can smoothly react with alcohols or amines to produce the corresponding esters or amides of 3-chlorobenzoic acid, respectively. It was found that the novel benziodazolone reagent reacts more efficiently than the analogous benziodoxolone reagent in this esterification.

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