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dimethyl bis[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]methyl]malonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39266-67-6

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39266-67-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39266-67-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,2,6 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 39266-67:
(7*3)+(6*9)+(5*2)+(4*6)+(3*6)+(2*6)+(1*7)=146
146 % 10 = 6
So 39266-67-6 is a valid CAS Registry Number.
InChI:InChI=1/C35H52O6/c1-31(2,3)23-15-21(16-24(27(23)36)32(4,5)6)19-35(29(38)40-13,30(39)41-14)20-22-17-25(33(7,8)9)28(37)26(18-22)34(10,11)12/h15-18,36-37H,19-20H2,1-14H3

39266-67-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2,2-bis[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]propanedioate

1.2 Other means of identification

Product number -
Other names dimethyl bis(3,5-di-tert-butyl-4-hydroxybenzyl)malonate

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:39266-67-6 SDS

39266-67-6Downstream Products

39266-67-6Relevant academic research and scientific papers

Salts of acyl halides and 3,5-di-tert-butyl-4-hydroxy-N,N-dimethylbenzylamine in benzylation reactions

Gorbunov, D. B.,Ershov, V. V.,Nikiforov, G. A.

, p. 481 - 485 (2007/10/02)

The interaction of 3,5-di-tert-butyl-4-hydroxy-N,N-dimethylbenzylamine with various acyl halides has been studied.The N-acyl quaternary salts obtained can be used to introdice a sterically hindered phenol fragment into organic compounds containing an active methylene group.

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