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35564-39-7

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35564-39-7 Usage

Classification

Pyrazolone derivative.

Uses

Reagent in biochemical assays, quantitative determination of hydrogen peroxide and peroxidase activity.

Medicinal properties

Analgesic, anti-inflammatory, and antipyretic effects.

Molecular structure

Pyrazolone ring with a methyl and amino group attached to the carbon atoms, and a phenyl ring linked to the nitrogen atom.

Importance

Significant chemical compound in scientific research and industrial settings.

Check Digit Verification of cas no

The CAS Registry Mumber 35564-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,5,6 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 35564-39:
(7*3)+(6*5)+(5*5)+(4*6)+(3*4)+(2*3)+(1*9)=127
127 % 10 = 7
So 35564-39-7 is a valid CAS Registry Number.

35564-39-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-amino-phenyl)-5-methyl-1,2-dihydro-pyrazol-3-one

1.2 Other means of identification

Product number -
Other names 2-(4-Amino-phenyl)-5-methyl-1,2-dihydro-pyrazol-3-on

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:35564-39-7 SDS

35564-39-7Relevant articles and documents

Pyrazolone methylamino piperidine derivatives as novel CCR3 antagonists

Pegurier, Cecile,Collart, Philippe,Danhaive, Pierre,Defays, Sabine,Gillard, Michel,Gilson, Frederic,Kogej, Thierry,Pasau, Patrick,Van Houtvin, Nathalie,Van Thuyne, Marc,van Keulen, BerendJan

, p. 4228 - 4231 (2008/02/09)

The discovery and optimization of a novel class of potent CCR3 antagonists is described. Details of synthesis and SAR are given together with some ADME properties of selected compounds. An optimal balance between activities, physicochemical properties, and in vitro metabolic stability was reached by the proper choice of substituents.

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