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59974-79-7

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59974-79-7 Usage

General Description

2-[(diphenylmethoxy)carbonyl]benzoic acid, also known as diphenylmethyl 2-((carboxymethoxy)carbonyl)benzoate, is a chemical compound with the molecular formula C21H18O4. It is a white solid that is soluble in organic solvents. 2-[(diphenylmethoxy)carbonyl]benzoic acid is often used in the synthesis of pharmaceuticals and has been studied for its potential as an antiviral and anticancer agent. It works by inhibiting the activity of certain enzymes and proteins in the body, making it a promising candidate for various therapeutic applications. Furthermore, its unique structure and properties make it a valuable tool for research in organic synthesis and medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 59974-79-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,9,7 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 59974-79:
(7*5)+(6*9)+(5*9)+(4*7)+(3*4)+(2*7)+(1*9)=197
197 % 10 = 7
So 59974-79-7 is a valid CAS Registry Number.

59974-79-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzhydryloxycarbonylbenzoic acid

1.2 Other means of identification

Product number -
Other names phthalic acid monobenzhydryl 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:59974-79-7 SDS

59974-79-7Relevant articles and documents

1,2,3,4-Tetrahydro-1-naphthyl ester as a selective protecting group for carboxylic acids

Slade, Christopher J.,Pringle, Carol A.,Sumner, Ian G.

, p. 5601 - 5604 (2007/10/03)

The carboxylic acid functionality can be protected as the 1,2,3,4- tetrahydro-1-naphthyl ester, which can be selectively cleaved in the presence of aryl and alkyl esters using chlorotrimethylsilane and sodium iodide in acetonitrile. This protecting group allows room temperature deprotection under essentially neutral conditions throughout the cleavage reaction.

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