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39205-91-9

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39205-91-9 Usage

Structure

A chemical compound containing a pyrazole ring and a carboxamide group, with a nitro group at the 3-position.

Classification

Organic compound

Usage

Intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds.

Properties

Known for its antimicrobial and anticancer properties and has potential use in the development of therapeutic drugs.

Role

Used in research and development as a building block in the synthesis of more complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 39205-91-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,2,0 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 39205-91:
(7*3)+(6*9)+(5*2)+(4*0)+(3*5)+(2*9)+(1*1)=119
119 % 10 = 9
So 39205-91-9 is a valid CAS Registry Number.

39205-91-9SDS

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 3-nitro-4-pyrazolecarboxamide

1.2 Other means of identification

Product number -
Other names 3-nitro-4-pyrazolecarboxamide

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:39205-91-9 SDS

39205-91-9Upstream product

39205-91-9Relevant articles and documents

Nitropyrazoles 5. Synthesis of substituted 3-nitropyrazoles from 3-amino-4-cyanopyrazole

Vinogradov, V. M.,Cherkasova, T. I.,Dalinger, I. L.,Shevelev, S. A.

, p. 1552 - 1554 (2007/10/02)

A preparative method of synthesis of 3-nitro-4-cyanopyrazole (1) from the available 3-amino-4-cyanopyrazole was developed.Chemical conversions of 1 were studied, and 3-nitro-4-R-pyrazoles (R = CO2H, CONH2, NHCO2Me, NH2, Br, NO2), as well as 3,5-dinitro-4-methoxycarbonylaminopyrazole were obtained starting from 1.

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