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89532-43-4

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89532-43-4 Usage

General Description

3-(1H-pyrazol-1-yl)propanal is a chemical compound that consists of a pyrazole ring, a three-carbon propanal chain, and a functional aldehyde group. It is commonly used as an intermediate in the synthesis of various organic compounds and pharmaceuticals. The presence of the pyrazole ring gives this compound unique chemical and biological properties, making it of interest to researchers in the fields of medicinal chemistry and drug development. Its potential uses include anti-inflammatory, analgesic, and antimicrobial properties, and it is also being studied for its potential as a therapeutic agent in the treatment of certain diseases and medical conditions. However, as with any chemical compound, proper handling and safety precautions should be taken when working with 3-(1H-pyrazol-1-yl)propanal.

Check Digit Verification of cas no

The CAS Registry Mumber 89532-43-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,3 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 89532-43:
(7*8)+(6*9)+(5*5)+(4*3)+(3*2)+(2*4)+(1*3)=164
164 % 10 = 4
So 89532-43-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H8N2O/c9-6-2-5-8-4-1-3-7-8/h1,3-4,6H,2,5H2

89532-43-4SDS

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-pyrazol-1-ylpropanal

1.2 Other means of identification

Product number -
Other names 3-pyrazol-1-yl-propionaldehyde

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:89532-43-4 SDS

89532-43-4Downstream Products

89532-43-4Relevant articles and documents

Structure of the products of acrolein reactions with pyrazoles

Attaryan,Antanosyan,Kinoyan,Tamazyan,Panosyan,Matsoyan

, p. 1868 - 1870 (2006)

-

Hafnium chloride catalyzed conjugate addition of pyrrole, pyrazole and imidazole to α,β-unsaturated ketones

Aburatani, Sachiko,Kawatsura, Motoi,Uenishi, Jun'ichi

, p. 189 - 196 (2008/02/02)

Pyrrole, pyrazole and imidazole undergo conjugate addition with α,β-unsaturated ketones in the presence of a catalytic amount of hafnium chloride at room temperature. Although the reaction of pyrrole gave 2,5-substituted C-adduct mainly, those of pyrazole

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