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1,3-Cyclohexanedione, 2-diazo-4,6-bis(1,1-dimethylethyl)-, cis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96144-03-5

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96144-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96144-03-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,1,4 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 96144-03:
(7*9)+(6*6)+(5*1)+(4*4)+(3*4)+(2*0)+(1*3)=135
135 % 10 = 5
So 96144-03-5 is a valid CAS Registry Number.

96144-03-5SDS

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-diazo-4,6-cis-di-tert-butyl-1,3-cyclohexanedione

1.2 Other means of identification

Product number -
Other names 2-diazo-cis-4,6-di-tert-butylcyclohexane-1,3-dione

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:96144-03-5 SDS

96144-03-5Relevant academic research and scientific papers

CHEMISTRY OF DIAZO DICARBONYL COMPOUNDS. X. SYNTHESIS, STEREOCHEMISTRY, AND WOLFF REARRANGMENT OF cis- AND trans-4,6-DI-TERT-BUTYL-2-DIAZOCYCLOHEXANE-1,3-DIONES

Nikolaev, V. A.,Korneev, S. M.,Terent'eva, I. V.,Korobistyna, I. K.

, p. 1845 - 1858 (2007/10/02)

Stereoisomeric cis- and trans-4,6-di-tert-butyl-2-diazocyclohexane-1,3-diones and their deuterated analogs (d2-4,6) were synthesized, a method for separating the stereoisomers was developed, and their configurations were established.The photoch

An improved synthesis of 2-diazo-1,3-diketones

Popic,Korneev,Nikolaev,Korobitsyna

, p. 195 - 198 (2007/10/02)

The sodium hydride/dibenzo-18-crown-6 ether system was found to be an effective base for the synthesis of 1,3-diketones by the Claisen condensation. The use of potassium fluoride (with or without crown ether) as the base in diazo-transfer reactions extends this reaction to the synthesis of hindered diazo diketones. In the case of isomeric 1,3-diketones, the stereoselectivity of the process considerably rises.

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