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3-butyl-2-hydroxy-6-methylpyridin-4(1H)-one is a complex organic compound belonging to the pyridinone family, characterized by a pyridine ring structure with a hydroxyl group at the 2nd position, a methyl group at the 6th position, and a butyl chain attached to the 3rd position. 3-butyl-2-hydroxy-6-methylpyridin-4(1H)-one is known for its potential applications in pharmaceuticals and agrochemicals, where it may exhibit biological activity. Its chemical structure provides a foundation for further research into its properties and possible uses, such as in the development of new drugs or as a chemical intermediate in the synthesis of other compounds.

6967-70-0

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6967-70-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6967-70-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,6 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6967-70:
(6*6)+(5*9)+(4*6)+(3*7)+(2*7)+(1*0)=140
140 % 10 = 0
So 6967-70-0 is a valid CAS Registry Number.

6967-70-0SDS

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 3-butyl-4-hydroxy-6-methyl-1H-pyridin-2-one

1.2 Other means of identification

Product number -
Other names 3-n-Butyl-2,4-dihydroxy-6-methyl-pyridin

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 -
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More Details:6967-70-0 SDS

6967-70-0Relevant academic research and scientific papers

Investigations on the Cyclization of Alkylmalonic Acid Esters with β-Aminocrotonic Acid Esters to Alkylated Hydroxypyridine Carboxylic Acid Esters

Schroetter, E.,Niedrich, H.,Schick, H.

, p. 619 - 624 (2007/10/02)

The cyclization of substituted malonic esters with β-aminocrotonic acid alkyl esters yields 2,4- or 4,6-dihydroxy-3-pyridinecarboxylic acid esters, respectively, in dependence on the reaction conditions and the nature of the substituent in the malonic esters.In the presence of alcoholate malonic acid alkyl esters and alkylmalonic acid alkyl esters form 2,4-dihydroxy-3-pyridine-carboxylic acid esters.Under the same conditions nitromalonic acid alkyl esters lead to 4,6-dihydroxy-3-pyridinecarboxylic acid esters, which also arise in the thermal cyclization of malonic acid 2,4,6-trichlorophenyl ester.The structure of the reaction products is determined by the relative nucleophilicity of the cyclization components.

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