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136285-36-4

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136285-36-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136285-36-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,2,8 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 136285-36:
(8*1)+(7*3)+(6*6)+(5*2)+(4*8)+(3*5)+(2*3)+(1*6)=134
134 % 10 = 4
So 136285-36-4 is a valid CAS Registry Number.

136285-36-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-nitro-2-(pentanoylamino)benzoate

1.2 Other means of identification

Product number -
Other names methyl 3-nitro-2-(N-valerylamino)benzoate

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:136285-36-4 SDS

136285-36-4Relevant articles and documents

Imidazopyridine derivatives as angiotensin II receptor antagonists, pharmaceuticals, and treatment of hypertension therewith

-

, (2008/06/13)

Imidazo-fused iso- and heterocycles, process for their preparation, compositions containing them and their useA compound of the formula STR1 in which the symbols have the following meaning: X is a monocyclic radical having 3,4 or 5 ring atoms,R 1,R 2,R 3,

Benzimidazole derivatives and their use

-

, (2008/06/13)

Novel imidazole derivatives of the formula (I): STR1 wherein R1 is an optionally substituted alkyl group, R2 and R3 are independently a group capable of forming an anion or a group which can be changed thereinto, ring A is a benzene ring optionally having, besides the group shown by R2, further substituents, and X shows linkage of phenylene group and phenyl group directly or through a spacer whose atomic length is not more than 2 and a salt thereof, show antagonistic actions to angiotensin II, thus being useful as therapeutics for cardiovascular diseases.

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