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61255-82-1

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61255-82-1 Usage

General Description

1H-Pyrazole-1-propanenitrile, 5-amino-3-methyl-(9CI) is a chemical compound with the molecular formula C6H8N4. It is a derivative of pyrazole and contains a nitrile group and an amino group. 1H-Pyrazole-1-propanenitrile,5-amino-3-methyl-(9CI) is mainly used in the pharmaceutical industry for the synthesis of various organic molecules. It is known for its wide range of biological activities, including anti-tumor, antibacterial, and antifungal properties. Additionally, it has been studied for its potential use in the treatment of various diseases, making it a valuable intermediate in organic synthesis and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 61255-82-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,5 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61255-82:
(7*6)+(6*1)+(5*2)+(4*5)+(3*5)+(2*8)+(1*2)=111
111 % 10 = 1
So 61255-82-1 is a valid CAS Registry Number.

61255-82-1SDS

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 3-(5-amino-3-methylpyrazol-1-yl)propanenitrile

1.2 Other means of identification

Product number -
Other names 5-Amino-3-methyl-1-(2-cyanoethyl)pyrazol

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:61255-82-1 SDS

61255-82-1Downstream Products

61255-82-1Relevant articles and documents

The reaction of amino-imidazoles, -pyrazoles and -triazoles with α,β-unsaturated nitriles

Komykhov, Sergey A.,Ostras, Konstantin S.,Kostanyan, Alvard R.,Desenko, Sergey M.,Orlov, Valery D.,Meier, Herbert

, p. 1111 - 1116 (2005)

The reactions of α,β-unsaturated nitriles (1, 9, 12) as bielectrophiles with aminoazoles (2, 4, 6) as binucleophiles were investigated. Acrylonitrile (1) reacts almost exclusively in a chemoselective Michael-type addition yielding the substituted azoles 3, 5 and 7, respectively. Cinnamonitriles 9a,b behave in a similar way, but the free CN group adds a second molecule 4 yielding 10a,b and its cyclocondensation product 11a,b as minor component. The attempted formation of azolopyrimidines is best achieved by the reaction of the benzylidenemalononitriles 12a - f with 2 or 4. The process is chemo- and regioselective. The structure determinations were based on NMR measurements including DEPT, COSY, ROESY, HMQC and HMBC techniques and correct earlier suggestions.

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