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10050-12-1

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10050-12-1 Usage

General Description

5-AMINO-2-(4-CHLORO-PHENYL)-2,4-DIHYDRO-PYRAZOL-3-ONE is a chemical compound with the molecular formula C10H10N2OCl. It is a pyrazolone derivative with a substituted phenyl group and an amino group attached to the pyrazolone ring. 5-AMINO-2-(4-CHLORO-PHENYL)-2,4-DIHYDRO-PYRAZOL-3-ONE has potential applications in pharmaceutical and agricultural industries due to its pharmacological and biological activities, such as anti-inflammatory properties. It may also possess antimicrobial and antifungal properties. Additionally, it has been studied for its potential use as a building block in the synthesis of other organic compounds. Overall, 5-AMINO-2-(4-CHLORO-PHENYL)-2,4-DIHYDRO-PYRAZOL-3-ONE is a versatile chemical with diverse potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 10050-12-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,5 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10050-12:
(7*1)+(6*0)+(5*0)+(4*5)+(3*0)+(2*1)+(1*2)=31
31 % 10 = 1
So 10050-12-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H8ClN3O/c10-6-1-3-7(4-2-6)13-9(14)5-8(11)12-13/h1-4H,5H2,(H2,11,12)

10050-12-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-amino-2-(4-chlorophenyl)-4H-pyrazol-3-one

1.2 Other means of identification

Product number -
Other names 5-Amino-2-(4-chloro-phenyl)-2,4-dihydro-pyrazol-3-one

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:10050-12-1 SDS

10050-12-1Upstream product

10050-12-1Downstream Products

10050-12-1Relevant articles and documents

A New Synthesis of 3-Amino-1-aryl-2-pyrazolin-5-ones

Hyatt, John A.,Maggiulli, Cataldo A.,French, Stephen E.

, p. 773 - 774 (2007/10/02)

Reaction of ethyl 3-nitropropionate with aryldiazonium chlorides in basic medium yields ethyl 3-nitro-3-(arylhydrazono)propionates.These α-nitrohydrazones are converted by catalytic hydrogenation to 3-amino-1-aryl-2-pyrazolin-5-ones, probably via cyclization of intermediate amidrazones produced in situ.This appears to be the first route to the title compounds that does not use a substituted phenyl hydrazine intermediate and offers advantages in the preparation of pyrazolinones bearing electron-rich aryl rings.

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