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di(tert-butyl) 4-hydroxy-4-methyl-6-oxo-2-phenyl-1,3-cyclohexanedicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96268-73-4

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96268-73-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96268-73-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,2,6 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 96268-73:
(7*9)+(6*6)+(5*2)+(4*6)+(3*8)+(2*7)+(1*3)=174
174 % 10 = 4
So 96268-73-4 is a valid CAS Registry Number.

96268-73-4SDS

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 2,4-bis(tert-butoxycarbonyl)-5-hydroxy-5-methyl-3-phenylcyclohexanone

1.2 Other means of identification

Product number -
Other names 4-Hydroxy-4-methyl-6-oxo-2-phenyl-cyclohexane-1,3-dicarboxylic acid di-tert-butyl ester

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:96268-73-4 SDS

96268-73-4Relevant academic research and scientific papers

Reaction of dialkyl 2-aryl-4-hydroxy-4-methyl-6-oxocyclohexane-1,3- dicarboxylates with aliphatic amines

Gein,Nosova,Prusakova,Vakhrin,Kriven'Ko

experimental part, p. 2357 - 2362 (2009/05/27)

Benzylamine, phenethylamine, and homoveratrylamine reacted with dialkyl 2-aryl-4-hydroxy-4-methyl-6-oxocyclohexane-1,3-dicarboxylates at the endocyclic carbonyl group with conservation of the enolic hydroxy group to give dialkyl 4-alkylamino-2-aryl-6-hydroxy-6-methylcyclohex-3-ene-1,3-dicarboxylates. The reaction of dimethyl 4-hydroxy-4-methyl-6-oxo-2-phenylcyclohexane-1,3- dicarboxylate with tryptamine was accompanied by dehydration with formation of dimethyl 4-[2-(1H-indol-3-yl)ethylamino]-6-methyl-2-phenylcyclohexa-3,5-diene-1, 3-dicarboxylate, presumably due to basic properties of the indole nitrogen atom.

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