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92929-53-8

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92929-53-8 Usage

General Description

5-Methyl-pyridazine-4-carboxylic acid ethyl ester is a chemical compound with the molecular formula C8H10N2O2. It is an ester formed from 5-methyl-pyridazine-4-carboxylic acid and ethanol. 5-METHYL-PYRIDAZINE-4-CARBOXYLIC ACID ETHYL ESTER is commonly used in organic synthesis and as an intermediate in the production of pharmaceuticals and agrochemicals. It has a faint, sweet, and fruity odor and is typically a colorless to pale yellow liquid. The compound is known to be irritating to the skin, eyes, and respiratory system and should be handled with caution in a laboratory setting.

Check Digit Verification of cas no

The CAS Registry Mumber 92929-53-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,2 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 92929-53:
(7*9)+(6*2)+(5*9)+(4*2)+(3*9)+(2*5)+(1*3)=168
168 % 10 = 8
So 92929-53-8 is a valid CAS Registry Number.

92929-53-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 5-methylpyridazine-4-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 5-methyl-4-pyridazinecarboxylate

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:92929-53-8 SDS

92929-53-8Relevant articles and documents

PYRIDAZINES XXIV. APPLICATION OF RADICALIC ETHOXYCARBONYLATION TO THE SYNTHESIS OF PYRIDAZINE MONO- AND POLYCARBOXYLIC ACID ESTERS

Heinisch, Gottfried,Loetsch, Gerhard

, p. 1199 - 1206 (2007/10/02)

Reactivity of pyridazines 1, 2, 3, 16 towards ethoxycarbonylradical (generated by redox decomposition of oxyhydroperoxyde of ethylpyruvate) was studied.Application of this type of homolytic substitution for synthesis of hitherto not accessible pyridazine carboxylic acid esters 6, 8, 9, 12, 13, 14, 15, 17 is demonstrated.In addition improved synthesis of diethyl 4,5-pyridazinedicarboxylate (5) is proposed.

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