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151521-41-4

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151521-41-4 Usage

Molecular weight

122.17 g/mol

Also known as

4-Propyl-1H-pyrazole-3-amine

Classification

Pyrazole derivative

Physical state

Colorless solid

Potential applications

Organic and pharmaceutical

Importance in medicinal chemistry

Building block for the synthesis of various bioactive molecules and pharmaceutical compounds

Significance of propyl group

Potential for use in the development of novel drugs and chemical compounds with specific properties and activities.

Check Digit Verification of cas no

The CAS Registry Mumber 151521-41-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,5,2 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 151521-41:
(8*1)+(7*5)+(6*1)+(5*5)+(4*2)+(3*1)+(2*4)+(1*1)=94
94 % 10 = 4
So 151521-41-4 is a valid CAS Registry Number.

151521-41-4SDS

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 3-amino-4-n-propyl-1H-pyrazole

1.2 Other means of identification

Product number -
Other names 4-Propyl-1H-pyrazol-3-amine

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:151521-41-4 SDS

151521-41-4Relevant articles and documents

Studies on nonpeptide angiotensin II receptor antagonists. I. Synthesis and biological evaluation of pyrazolo [1,5-b][1,2,4]triazole derivatives with alkyl substituents

Okazaki, Toshio,Suga, Akira,Watanabe, Toshihiro,Kikuchi, Kazumi,Kurihara, Hiroyuki,Shibasaki, Masayuki,Fujimori, Akira,Inagaki, Osamu,Yanagisawa, Isao

, p. 69 - 78 (2007/10/03)

Alkyl-substituted pyrazolo[1,5-b][1,2,4]triazole derivatives were synthesized and evaluated for activity as angiotensin II receptor antagonists. Molecules with the (methylbiphenylyl)tetrazole moiety at N-5 were the preferred compounds. Ethyl substitutions

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