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[Bi-1-cyclohexen-1-yl]-6,6'-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95251-70-0

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95251-70-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95251-70-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,2,5 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 95251-70:
(7*9)+(6*5)+(5*2)+(4*5)+(3*1)+(2*7)+(1*0)=140
140 % 10 = 0
So 95251-70-0 is a valid CAS Registry Number.

95251-70-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2'-bis(2-cyclohexen-1-one)

1.2 Other means of identification

Product number -
Other names 2,2'-Dioxo-dicyclohexen-(6)-yl

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:95251-70-0 SDS

95251-70-0Relevant academic research and scientific papers

Selective cross-coupling of organic halides with allylic acetates

Anka-Lufford, Lukiana L.,Prinsell, Michael R.,Weix, Daniel J.

, p. 9989 - 10000 (2013/01/15)

A general protocol for the coupling of haloarenes with a variety of allylic acetates is presented. Strengths of the method are a tolerance for electrophilic (ketone, aldehyde) and acidic (sulfonamide, trifluoroacetamide) substrates and the ability to couple with a variety of substituted allylic acetates. Secondary alkyl bromides can also be allylated under slightly modified conditions, demonstrating the generality of the approach. Finally, the coupling of a reactive vinyl halide could be achieved by the use of a very hindered ligand and more reactive, branched allylic acetates.

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