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91374-54-8

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91374-54-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91374-54-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,3,7 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91374-54:
(7*9)+(6*1)+(5*3)+(4*7)+(3*4)+(2*5)+(1*4)=138
138 % 10 = 8
So 91374-54-8 is a valid CAS Registry Number.

91374-54-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(3,5-di-tert-butyl-4-hydroxybenzyl)-3-methyl-2-cyclohexen-1-one

1.2 Other means of identification

Product number -
Other names 6-(3,5-Di-tert-butyl-4-hydroxy-benzyl)-3-methyl-cyclohex-2-enone

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:91374-54-8 SDS

91374-54-8Relevant articles and documents

C-ALKYLATION OF PHENOLS WITH METHYL VINYL KETONE IN THE PRESENCE OF BASES

Titova, T. F.,Krysin, A. P.,Shakirov, M. M.,Mamatyuk, V. I.

, p. 294 - 301 (2007/10/02)

The C-alkylation of phenols with methyl vinyl ketone in alcohols in the presence of alkali-metal alcoholates at -60 to +40 deg C was investigated by the PMR method.At -30 to 0 deg C methyl vinyl ketone reacts with primary alcohols with the formation of β-alkoxy-2-butanones, the subsequent reaction of which with 2,6-di-tert-butylphenol at 20-40 deg C by a mechanism of nucleophilic substitution leads to the formation of 4-(3,5-di-tert-butyl-4-hydroxyphenyl)-2-butanone.The composition of the products from the reaction of 2,6-di-tert-butylphenol with methyl vinyl ketone and β-methoxy-2-butanone was studied.

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