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1177300-40-1

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1177300-40-1 Usage

General Description

3-(1H-pyrazol-1-yl)propanohydrazide, also known as SALTDATA: FREE, is a chemical compound with the molecular formula C6H10N4O. It is a hydrazide derivative of 1H-pyrazole, and it is commonly used in pharmaceutical research and drug discovery. 3-(1H-pyrazol-1-yl)propanohydrazide(SALTDATA: FREE) has been studied for its potential biological and pharmacological activities, including its potential as an antiviral and antitumor agent. It is also being investigated for its potential use in the treatment of various diseases and medical conditions. Additionally, 3-(1H-pyrazol-1-yl)propanohydrazide may have other industrial and research applications, making it an important chemical in various scientific and medical fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1177300-40-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,7,3,0 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1177300-40:
(9*1)+(8*1)+(7*7)+(6*7)+(5*3)+(4*0)+(3*0)+(2*4)+(1*0)=131
131 % 10 = 1
So 1177300-40-1 is a valid CAS Registry Number.

1177300-40-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1H-Pyrazol-1-yl)propanohydrazide

1.2 Other means of identification

Product number -
Other names 3-pyrazol-1-ylpropanehydrazide

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:1177300-40-1 SDS

1177300-40-1Relevant articles and documents

Synthesis of N- and C-azolyl-substituted pyrazolo[1,5-a]pyrimidines by recyclization of pyrimidinium salts

Danagulyan, Gevorg G.,Tumanyan, Araksya K.,Attaryan, Oganes S.,Tamazyan, Rafael A.,Danagulyan, Anna G.,Ayvazyan, Armen G.

, p. 483 - 490 (2015/10/19)

We studied the reaction of 2-(ethoxycarbonyl)methyl-1,4,6-trimethylpyrimidinium iodide with hydrazides of N-azolyl- and C-pyrazolyl-substituted carboxylic acids, which were synthesized by reacting the respective esters with hydrazine hydrate. This reaction was shown to result in recyclization and formation of ethyl 2-(pyrazolylalkyl)- and 2-(azolylalkyl)-5,7-dimethylpyrazolo[1,5-a]pyrimidine- 3-carboxylates. Besides pyrazolopyrimidines, the separation of reaction mixture provided in some cases also another recyclization product, 2-hydroxy-5,7-dimethylpyrazolo[1,5-a]pyrimidine.

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