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Cyclohexanone, 2-(1,1-dimethylethyl)-2-hydroxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88264-36-2

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88264-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88264-36-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,6 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88264-36:
(7*8)+(6*8)+(5*2)+(4*6)+(3*4)+(2*3)+(1*6)=162
162 % 10 = 2
So 88264-36-2 is a valid CAS Registry Number.

88264-36-2SDS

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 2-tert-butyl-2-hydroxycyclohexan-1-one

1.2 Other means of identification

Product number -
Other names 2-tert-Butyl-2-hydroxy-1-cyclohexanon

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:88264-36-2 SDS

88264-36-2Downstream Products

88264-36-2Relevant academic research and scientific papers

Regioselective Lewis Acid-mediated α-tert-Alkylation of Acyloins and Glycolic Acid

Reetz, Manfred T.,Heimbach, Horst

, p. 3702 - 3707 (2007/10/02)

O,O'-Bis-silylated acyloins 10a-h as well as the tris-silylated form 13 of glycolic acid (7) can be tert-alkylated with tert-butyl chloride or 1-adamantyl bromide in the presence of catalytic amounts of ZnCl2.In case of unsymmetrically substituted derivatives, complete regioselectivity according to the Markovnikov rule is observed.The adamantylated acyloins are converted into α,β-unsaturated α-adamantyl ketones 27-30 upon treatment with H2SO4.

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