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62639-21-8

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62639-21-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62639-21-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,3 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62639-21:
(7*6)+(6*2)+(5*6)+(4*3)+(3*9)+(2*2)+(1*1)=128
128 % 10 = 8
So 62639-21-8 is a valid CAS Registry Number.

62639-21-8SDS

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 4-hydroxy-N-(2-methylphenyl)benzamide

1.2 Other means of identification

Product number -
Other names 4-Hydroxy-benzoesaeure-<2-methyl-anilid>CTK2B5421

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:62639-21-8 SDS

62639-21-8Relevant articles and documents

Aryl alkyl ether compound as well as derivative, preparation method, pharmaceutical composition and application thereof

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, (2021/05/12)

The invention discloses an aryl alkyl ether compound as well as a derivative, a preparation method, a pharmaceutical composition and application thereof. The structure of the aryl alkyl ether compound is shown as a formula (I). The aryl alkyl ether compound derivative relates to a stereoisomer, a tautomer, a metabolite, a metabolic precursor, a prodrug, a solvate, a salt of the solvate, a crystal, a pharmaceutically acceptable salt or a mixture of the stereoisomer, the tautomer, the metabolite, the metabolic precursor, the prodrug and the solvate of the aryl alkyl ether compound. The aryl alkyl ether compound and the derivative thereof have a remarkable inhibition effect on indoleamine 2, 3-dioxygenase 1, and can be used for preparing a medicine for treating indoleamine 2, 3-dioxygenase 1 mediated immunosuppression related diseases, and the prepared medicine can exert the medicine effect at the molecular level and is wide in application.

COMPARATIVE STUDIES ON THE PREPARATION OF ISOMERIC HYDROXYBENZAMIDES.

SCHOENENBERGER,HOLZHEU-ECKARDT,BAMANN

, p. 324 - 328 (2007/10/05)

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