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3,3-bis(3-tert-butyl-4-hydroxyphenyl)butyric acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32509-69-6

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32509-69-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32509-69-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,5,0 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 32509-69:
(7*3)+(6*2)+(5*5)+(4*0)+(3*9)+(2*6)+(1*9)=106
106 % 10 = 6
So 32509-69-6 is a valid CAS Registry Number.

32509-69-6Relevant academic research and scientific papers

Preparation method of hindered phenol antioxidant and intermediate thereof

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Paragraph 0051-0066, (2020/10/04)

The invention provides a preparation method of a hindered phenol antioxidant and an intermediate thereof. The preparation method comprises the following steps of: carrying out Friedel-Crafts reactionon a compound a and a compound b under the action of a main catalyst organic sulfonic acid and/or trifluoroacetic acid and a cocatalyst to obtain a hindered phenol antioxidant intermediate shown as aformula I; wherein the structural formulas of the compound a, the compound b and formula I are shown as the specification, wherein R1 is selected from H and substituted or unsubstituted alkyl of C1-C4, and R2 is selected from substituted or unsubstituted alkyl of C1-C4. According to the preparation of the hindered phenol antioxidant intermediate, the organic sulfonic acid and/or trifluoroacetic acid are/is adopted to replace a hydrogen chloride gas catalyst, so that the reaction safety is greatly improved, the requirements on equipment are reduced, and the equipment cost is also reduced.

Process for the preparation a bis(3,3-bis(4-hydroxyalkylphenyl)butanoic acid)diol ester

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, (2008/06/13)

By dividing the known condensation of acetoacetic acid diol esters with phenols into two process steps, a reduction in the cost of the entire process can be achieved. Methyl acetoacetate is first condensed with a phenol and the methyl 3,3-bis(4-hydroxyalkylphenyl)butanoate formed is reacted with the desired diol in the presence of a transesterification catalyst. In this way only one acetoacetic ester is necessary for various final products. The final products are useful stabilizers for plastics, in particular polyolefins.

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