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89486-57-7

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89486-57-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89486-57-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,4,8 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 89486-57:
(7*8)+(6*9)+(5*4)+(4*8)+(3*6)+(2*5)+(1*7)=197
197 % 10 = 7
So 89486-57-7 is a valid CAS Registry Number.

89486-57-7SDS

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 trans-2-phenyl-1-(2-methyl-1-propenyl)cyclopropane

1.2 Other means of identification

Product number -
Other names [(1S,2R)-2-(2-Methyl-propenyl)-cyclopropyl]-benzene

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:89486-57-7 SDS

89486-57-7Downstream Products

89486-57-7Relevant articles and documents

The Heterogeneous Catalytic Hydrogenation of Cumulated Allene-cyclopropanes: 1-(2'-Methylpropenylidene)-2-phenylcyclopropane.

Cromble, Leslie,Fernando, Candida E. C.

, p. 1519 - 1537 (2007/10/03)

The unsymmetrical title compound 2 having phenyl as an activating substituent was hydrogenated in heterogeneous solution phase using supported platinum and palladium as well as Raney nickel catalysts. Data are presented graphically using 'snapshot analysi

Conversion of non-activated alkenes into cyclopropanes with lithiated sulfones under nickel catalysis

Gai, Yonghua,Julia, Marc,Verpeaux, Jean-Noel

, p. 817 - 829 (2007/10/03)

Summary -Lithiated alkyl ierf-butyl sulfones convert alkenes into cyclopropane derivatives under nickel catalysis. The new reaction appears to differ from the known cyclopropanation reactions from both the stereochemical and the electronic points of view. Elsevier.

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