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76606-68-3

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76606-68-3 Usage

Chemical Class

Pyrazole derivatives

Structural Feature

Pyrazole ring substituted with a 3,4-dichlorophenyl group and a methyl group

Potential Applications

Pharmaceutical industry

Biological Activity

Inhibitor of specific enzymes

Preclinical Research

Promise for treatment of certain diseases

Importance

Building block for synthesis of novel pharmaceuticals and bioactive compounds, valuable asset in medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 76606-68-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,6,0 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76606-68:
(7*7)+(6*6)+(5*6)+(4*0)+(3*6)+(2*6)+(1*8)=153
153 % 10 = 3
So 76606-68-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H9Cl2N3/c1-6-4-10(13)15(14-6)7-2-3-8(11)9(12)5-7/h2-5H,13H2,1H3

76606-68-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,4-dichlorophenyl)-5-methylpyrazol-3-amine

1.2 Other means of identification

Product number -
Other names -

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:76606-68-3 SDS

76606-68-3Relevant articles and documents

Amidinosemicarbazido derivatives of pyrazole: Synthesis and inhibitory effect on blood coagulation and platelet aggregation

Ferroni,Milani,Simoni,Orlandini,Poli,Guarneri

, p. 891 - 899 (2007/10/02)

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Pyrazolyl amino imidazolines as antihypertensive agents

-

, (2008/06/13)

Described is a method of treating hypertensive by administering to mammalian patients compounds of the formula STR1 wherein R1 and R2 are hydrogen, loweralkyl, lowercycloalkyl, aralkyl, aryl, pyridyl, isoquinolyl, phthalazinyl, or aryl substituted by one or more hydrogen, halo, loweralkyl, lowercycloalkyl, haloloweralkyl, haloloweralkyl, aminosulfonyl, nitro, hydroxy, alkoxy, carboxy, alkoxycarbonyl, cycloalkoxy carbonyl, aminocarbonyl, diloweralkylaminocarbonyl or STR2 wherein n is 4 or 5. R3 is hydrogen, halogen, loweralkyl or aryl, and R4 is hydrogen, acyl, amino or loweralkyl, and the pharmaceutically acceptable acid addition salts thereof.

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