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3920-41-0

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3920-41-0 Usage

Physical state

Yellow solid

Usage

Research and development

Application

Building block for the synthesis of pharmaceutical compounds and agrochemicals

Known for

Potential use as a precursor in the synthesis of various pyrazole derivatives

Industry relevance

Pharmaceutical industry and organic chemistry

Other potential applications

Industrial and research applications due to unique chemical properties and potential reactivity in various chemical reactions

Check Digit Verification of cas no

The CAS Registry Mumber 3920-41-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,2 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3920-41:
(6*3)+(5*9)+(4*2)+(3*0)+(2*4)+(1*1)=80
80 % 10 = 0
So 3920-41-0 is a valid CAS Registry Number.

3920-41-0SDS

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 1,5-dimethyl-4-nitropyrazole-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1.5-Dimethyl-4-nitro-pyrazol-3-carbonsaeure

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:3920-41-0 SDS

3920-41-0Relevant articles and documents

Synthesis and antitumor activity of a new class of pyrazolo[4,3- e]pyrrolo[1,2-a][1,4]diazepinone analogues of pyrrolo[1,4][2,1- c]benzodiazepines

Baraldi,Leoni,Cacciari,Manfredini,Simoni,Bergomi,Menta,Spinelli

, p. 4329 - 4337 (2007/10/02)

A new class of pyrrolo[1,4]benzodiazepine (PBD) analogues featuring a pyrazolo[4,3-e]pyrrolo[1,2-a][1,4]diazepinone ring system has been designed and synthesized. These compounds, 2a-o, are characterized by the substitution of the aromatic A ring, characteristic of the PBDs, with a disubstituted pyrazole ring bearing alkyl and benzyl substituents at N6 or N7 and alkyl or carbomethoxy substituents at C8. Biological evaluation revealed an appreciable in vitro cytotoxic activity for compounds 2a,b,f-i.

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