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108444-24-2

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108444-24-2 Usage

Class

Pyrazole derivative

Biological activities

Diverse

Potential applications

Pharmaceuticals and agrochemicals

Structural features

Carboxylic acid and methyl groups

Functional groups

Carboxylic acid and methyl groups

Pharmacological properties

Likely to be studied

Pesticidal properties

Likely to be studied

Intermediate in synthesis

Potential use in the synthesis of other organic compounds

Research and development

May be of interest for further research and development in various industries

Check Digit Verification of cas no

The CAS Registry Mumber 108444-24-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,4,4 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 108444-24:
(8*1)+(7*0)+(6*8)+(5*4)+(4*4)+(3*4)+(2*2)+(1*4)=112
112 % 10 = 2
So 108444-24-2 is a valid CAS Registry Number.

108444-24-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethyl-3,5-dimethylpyrazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names BB_SC-4255

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:108444-24-2 SDS

108444-24-2Downstream Products

108444-24-2Relevant articles and documents

Electrosynthesis of pyrazole-4-carboxylic acids by oxidation of 4-formylpyrazoles on NiO(OH)-electrode in aqueous alkaline solution

Lyalin,Petrosyan

, p. 1148 - 1153 (2013/07/26)

Electrochemical oxidation of di- and trisubstituted 4-formylpyrazoles on a Ni-anode in aqueous alkali led to the formation of the corresponding pyrazole-4-carboxylic acid in 60-90% yields. The yields of the target products depend on position of substituent in the pyrazole ring and are decreased in the following sequence of substituent at position 1 Me > Et > Ph, as well as when the aqueous medium was replaced with aqueous alcohol (50% Bu tOH). Oxidation of 4-formylpyrazoles containing Me groups at the carbon atoms of the pyrazole ring led, to monoacids and also pyrazoledicarboxylic acids in small (1.5-14%) amounts; the latter were the oxidation products of the aldehyde and the Me groups.

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