64210-57-7

Basic information

• Product Name: 3-Pyridazinecarboxylicacid,6-methyl-,ethylester(9CI)
• Synonyms: 3-Pyridazinecarboxylicacid,6-methyl-,ethylester(9CI);Ethyl 6-Methylpyridazine-3-carboxylate;6-methyl-3-Pyridazinecarboxylic acid ethyl ester
• CAS NO: 64210-57-7
• Molecular Formula: C8H10N2O2
• Molecular Weight: 166.18
• Product Categories: GLYCINESCAFFOLD
• Mol File: 64210-57-7.mol

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3-Pyridazinecarboxylicacid,6-methyl-,ethylester(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Pyridazinecarboxylicacid,6-methyl-,ethylester(9CI)(64210-57-7)
• EPA Substance Registry System: 3-Pyridazinecarboxylicacid,6-methyl-,ethylester(9CI)(64210-57-7)

Safety Data

• Hazardous Substances Data: 64210-57-7(Hazardous Substances Data)

Usage

Uses

Used in Chemical Research:
3-Pyridazinecarboxylic acid, 6-methyl-, ethyl ester (9CI) is used as a research compound for studying its chemical properties and potential applications in the field of organic chemistry. Its unique structure and characteristics make it a valuable subject for scientific investigation.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-Pyridazinecarboxylic acid, 6-methyl-, ethyl ester (9CI) is used as a starting material or intermediate in the synthesis of various pharmaceutical compounds. Its versatile structure allows for the development of new drugs with potential therapeutic applications.
Used in Material Science:
3-Pyridazinecarboxylic acid, 6-methyl-, ethyl ester (9CI) is also used in material science for the development of new materials with specific properties. Its incorporation into polymers or other materials can lead to the creation of novel materials with improved characteristics, such as enhanced stability or reactivity.
It is important to handle 3-Pyridazinecarboxylic acid, 6-methyl-, ethyl ester (9CI) with care and ensure it is stored properly to prevent any potential harm or reactions, as it is a chemical compound with potential hazards.

Upstream product

• 497-19-8 sodium carbonate 
• 64210-60-2 6-methyl-3-pyridazinecarboxylic acid 
• 107-06-2 1,2-dichloro-ethane 
• 35490-05-2 2-acetyl-5-oxohexanoic acid ethyl ester 
• 7803-57-8 hydrazine hydrate 

Downstream Products

• 848774-93-6 (6-methylpyridazin-3-yl)methanol 

Relevant articles and documents

SYNTHESIS OF FURAN, THIOPHENE, AND PYRROLES FROM ACETOACETIC ESTERS

The present invention refers to using ester pgd2 alkylacetoacetoates furan, thiophene, method relates to synthesis of pyrrole, more particularly the acetohydroxy pgd2 ester compound alpha, beta unsaturated carbonyl compounds obtained is added to the 1,5-dicarbonyl compounds (II)/ cobalt manganese (III) method of silica glass by sol the reaction deacetylase with Neel step then alkali to thereby synthesize a compound 1,4-dicarboxylic, Paal-Knorr herein using synthesis on the furan, thiophene, pyrrole for synthesizing relates to method. According to the present invention, a necessary for synthesis of Paal-Knorr 1,4-dicarbonyl compounds efficiently mixed in the oxidation reaction from said 1,5-dicarbonyl compounds (deacetylase reaction) and a conjunction synthesis on the Paal-Knorr in the reaction vessel a are sequentially two reactors furan, thiophene, and of won-port synthesis method by using the mask pattern.. (by machine translation)

Tandem catalytic oxidative deacetylation of acetoacetic esters and heteroaromatic cyclizations

One pot syntheses of furan, thiophene, and pyrrole were accomplished by oxidative deacetylation using Mn(iii)/Co(ii) catalysts and the Paal-Knorr reaction from 1,5-dicarbonyl compounds, which are prepared from the conjugate addition of ethyl acetoacetate to α,β-unsaturated carbonyl compounds. The oxidative deacetylation and reductive cyclization of β-ketoesters derived from ethyl acetoacetate and o-nitrobenzyl bromides efficiently produced diversely substituted indoles. This journal is

Derivatives of 1,2-dithiole and anti-bilharzia compositions thereof

1,2-Dithiole derivatives of the formula: STR1 wherein Het represents a pyridazin-3-yl radical, or a pyrimidin-2-yl, -4-yl or -5-yl radical, each such radical being optionally substituted by a halogen atom or by an alkyl radical of 1 through 4 carbon atoms, an alkoxy radical of 1 through 4 carbon atoms, the mercapto radical, an alkylthio radical of 1 through 4 carbon atoms or a dialkylamino group having 1 through 4 carbon atoms in each alkyl radical, are new compounds useful in the treatment of bilharziasis and amoebiases.

1,2-Dithiole derivatives

1,2-Dithiole derivatives of the formula: STR1 WHEREIN Het represents an aromatic heterocyclic radical with six atoms in the ring two of which are nitrogen atoms, the heterocyclic radical optionally carrying a single substituent selected from halogen, alkyl, alkoxy, mercapto, alkylthio, dialkylamino, pyrrolidin-1-yl, piperidino, morpholino and 4-alkylpiperazin-1-yl and R represents halogen, alkyl (optionally substituted by alkoxycarbonyl), carboxy, alkoxycarbonyl, carbamoyl, N-alkylcarbamoyl or a group R1 --C(OH)-- in which R1 represents hydrogen or alkyl, the said alkyl, alkoxy and alkylthio radicals or alkyl or alkoxy moieties containing 1 to 4 carbon atoms except in the case of R1 which contains 1 to 3 carbon atoms when an alkyl radical, are new compounds useful in the treatment of bilharziasis.