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130747-83-0

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130747-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130747-83-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,7,4 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 130747-83:
(8*1)+(7*3)+(6*0)+(5*7)+(4*4)+(3*7)+(2*8)+(1*3)=120
120 % 10 = 0
So 130747-83-0 is a valid CAS Registry Number.

130747-83-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-cyclohexylidene-3-methylbutane-1,3-diol

1.2 Other means of identification

Product number -
Other names 2-cyclohexylidene-3-methyl-1,3-butanediol

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:130747-83-0 SDS

130747-83-0Downstream Products

130747-83-0Relevant articles and documents

Radical Cyclization of (Bromomethyl)dimethylsilyl Propargyl Ethers. Regio-, Chemo-, and Stereoselectivity

Journet, Michel,Malacria, Max

, p. 3085 - 3093 (2007/10/02)

Radical cyclization of (bromomethyl)dimethylsilyl propargyl ether derivatives 1 is a powerful reaction with a high degree of regio-, chemo-, and stereoselectivity.Trisubstituted olefins 3, cyclopentene derivatives 5, and diquinane system 7j are obtained in good yields by a judicious choice of unsaturated substituents.Triquinane frameworks could be obtained stereoselectively from a suitable acyclic substrate of type 1 in a one-pot reaction.First attempts have not yet allowed us to aim at this goal due to interesting (1,5) hydrogen transfers.Moreover, we have intercepted, for the first time, the α-cyclopropyl radical which is involved in the Storck-Beckwith mechanism of the 5-versus 6-membered ring formation in the vinyl radical cyclization.

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