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199682-75-2

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199682-75-2 Usage

Type of compound

a pyrazole derivative with a carboxaldehyde functional group and a 2-methylpropyl substituent

Use in chemical synthesis

has applications in the pharmaceutical and agricultural industries

Listing in the Chemical Abstracts Service (CAS) database

9CI notation

Value in chemical processes and products

its properties and potential uses make it a valuable component

Check Digit Verification of cas no

The CAS Registry Mumber 199682-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,6,8 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 199682-75:
(8*1)+(7*9)+(6*9)+(5*6)+(4*8)+(3*2)+(2*7)+(1*5)=212
212 % 10 = 2
So 199682-75-2 is a valid CAS Registry Number.

199682-75-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(2-methylpropyl)-1H-pyrazole-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 3-ISOBUTYL-1H-PYRAZOLE-4-CARBALDEHYDE

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:199682-75-2 SDS

199682-75-2Downstream Products

199682-75-2Relevant articles and documents

Vilsmeier formylation of hydrazones and semicarbazones derived from alkyl, benzyl, and cycloalkyl methyl ketones

Lebedev,Lebedeva,Sheludyakov,Kovaleva,Ustinova,Kozhevnikov

, p. 412 - 416 (2007/10/03)

Formylation of ten accessible phenylhydrazones and semicarbazones derived from alkyl, benzyl, and cycloalkyl methyl ketones with the complex of POCl 3 with dimethylformamide was studied. Depending on the electronic and steric structure of the substrates, the reaction yields 1-phenyl- or 1-unsubstituted 3,4-dialkyl-, 3-alkyl-4-aryl-, or 3-alkyl-4-formylpyrazoles. These compounds can be readily oxidized into the corresponding carboxylic acids. 2005 Pleiades Publishing, Inc.

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