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71998-90-8

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71998-90-8 Usage

Chemical structure

A pyrazole derivative with a sulfonyl group attached to the phenyl ring

Enzyme inhibition

The compound has been studied for its potential as an enzyme inhibitor

Anti-inflammatory properties

It has been investigated for its possible anti-inflammatory effects

Pharmaceutical drugs

The compound may have applications in the development of pharmaceutical drugs

Medicinal chemistry

Its structure and properties make it a subject of interest for further research in medicinal chemistry

Drug discovery

The compound is also of interest for research in the field of drug discovery

Research focus

The compound's structure and properties make it a subject of interest for further research in the fields of medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 71998-90-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,9,9 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 71998-90:
(7*7)+(6*1)+(5*9)+(4*9)+(3*8)+(2*9)+(1*0)=178
178 % 10 = 8
So 71998-90-8 is a valid CAS Registry Number.

71998-90-8SDS

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 2-(benzenesulfonyl)-3,4-dihydropyrazol-5-amine

1.2 Other means of identification

Product number -
Other names 1-benzenesulfonyl-4,5-dihydro-1H-pyrazol-3-ylamine

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:71998-90-8 SDS

71998-90-8Relevant articles and documents

Reaction of 3-aminopyrazolines with nitrous acid. Stable nonaromatic diazonium salts.

Gorelik, M. V.,Titova, S. P.,Rybinov, V. I.

, p. 1143 - 1148 (2007/10/02)

During the action of a constant excess of nitrous acid on 1-phenyl-3-amino-Δ2-pyrazoline the initially formed cation-radical does not undergo dimerization but changes into a 1-phenyl-3-pyrazolediazonium salt.In the case of 1-(p-tolyl)-3-amino-Δ

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