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1-(2-CHLOROBENZYL)-1H-PYRAZOL-5-AMINE is a chemical compound that belongs to the pyrazole family. It is a derivative of pyrazole with a benzyl group and a chloro substituent. Pyrazoles are known for their diverse pharmacological properties, including anti-inflammatory, analgesic, and antipyretic effects. The introduction of a chloro group in the benzyl moiety can potentially modulate the biological activity of the compound.

3524-28-5

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3524-28-5 Usage

Uses

Used in Drug Development:
1-(2-CHLOROBENZYL)-1H-PYRAZOL-5-AMINE is used as a potential candidate in drug development for the treatment of various diseases and conditions. Its diverse pharmacological properties, including anti-inflammatory, analgesic, and antipyretic effects, make it a promising compound for further research and development.
Used in Medicinal Chemistry:
1-(2-CHLOROBENZYL)-1H-PYRAZOL-5-AMINE is used in medicinal chemistry to explore its full scope of pharmacological and therapeutic properties. The introduction of a chloro group in the benzyl moiety can potentially modulate the biological activity of the compound, making it a valuable tool for the development of new drugs and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 3524-28-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,2 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3524-28:
(6*3)+(5*5)+(4*2)+(3*4)+(2*2)+(1*8)=75
75 % 10 = 5
So 3524-28-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H10ClN3/c11-9-4-2-1-3-8(9)7-14-10(12)5-6-13-14/h1-6H,7,12H2

3524-28-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2-chlorophenyl)methyl]pyrazol-3-amine

1.2 Other means of identification

Product number -
Other names 1-(2'-chlorobenzyl)-5-aminopyrazole

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:3524-28-5 SDS

3524-28-5Downstream Products

3524-28-5Relevant academic research and scientific papers

TETRAZOLE COMPOUNDS AS OREXIN RECEPTOR ANTAGONISTS

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Page/Page column 18, (2011/04/25)

The invention relates to tetrazole compounds of formula (I) wherein X, Y, Z, R1, R2 and R3 are as described in the description; to pharmaceutically acceptable salts thereof, and to the use of such compounds use as medicaments, especially as orexin receptor antagonists.

Approach to the library of fused pyridine-4-carboxylic acids by combes-type reaction of acyl pyruvates and electron-rich amino heterocycles

Volochnyuk, Dmitriy M.,Ryabukhin, Sergey V.,Plaskon, Andrey S.,Dmytriv, Yuri V.,Grygorenko, Oleksandr O.,Mykhailiuk, Pavel K.,Krotko, Dmitriy G.,Pushechnikov, Alexei,Tolmachev, Andrey A.

scheme or table, p. 510 - 517 (2010/09/05)

A library of fused pyridine-4-carboxylic acids (including pyrazolo[3,4-b]pyridines, isoxazolo[5,4-b]pyridines, furo[2,3-b]pyridines, thieno[2,3-b]pyridines, and pyrido[2,3-d]pyrimidines) was generated by Combes-type reaction of acyl pyruvates and electron-rich amino heterocycles followed by hydrolysis of the ester. The library members were also demonstrated to undergo the standard combinatorial transformations including amide coupling and esterification, as well as less common heterocyclizations to 1,2,4-triazoles and 1,2,4-oxadiazoles.

TETRAZOLE COMPOUNDS AS OREXIN RECEPTOR ANTAGONISTS

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Page/Page column 44, (2010/01/07)

The invention relates to tetrazole compounds of formula (I) wherein X, Y, Z, R1, R2 and R3 are as described in the description; to pharmaceutically acceptable salts thereof, and to the use of such compounds use as medicaments, especially as orexin receptor antagonists.

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