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Heptanal, 2,3-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91526-44-2

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91526-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91526-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,5,2 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91526-44:
(7*9)+(6*1)+(5*5)+(4*2)+(3*6)+(2*4)+(1*4)=132
132 % 10 = 2
So 91526-44-2 is a valid CAS Registry Number.

91526-44-2Downstream Products

91526-44-2Relevant academic research and scientific papers

Method for Producing Isononanoic Acid Esters, Starting from 2-Ethyl Hexanol

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Paragraph 0077-0080; 0083, (2015/06/17)

A Process for preparing carboxylic esters of a mixture of structurally branched C9 monocarboxylic acids proceeding from 2-ethylhexanol is characterized in that (a) 2-ethylhexanol is dehydrated to an octene mixture in the presence of a catalyst; (b) the octene mixture obtained in step a) is reacted in the presence of a transition metal compound of group VIII of the periodic table of the elements with carbon monoxide and hydrogen to give a mixture of isomeric isononanals; (c) the mixture of isomeric isononanals obtained in step b) is oxidized to a mixture of structurally branched C9 monocarboxylic acids; and (d) the mixture of structurally branched C9 monocarboxylic acids obtained in step c) is reacted with alcohols to give carboxylic esters.

Method for Producing Isononanoic Acids from 2-Ethyl Hexanol

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Paragraph 0062-0068, (2015/07/15)

Process for preparing isononanoic acid proceeding from 2-ethylhexanol, characterized in that (a) 2-ethylhexanol is dehydrated to octene in the presence of a catalyst; (b) the octene obtained in step a) is reacted in the presence of a transition metal compound of group VIII of the periodic table of the elements with carbon monoxide and hydrogen to give isononanal; and (c) the isononanal obtained in step b) is oxidized to isononanoic acid.

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