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71194-27-9

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71194-27-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71194-27-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,1,9 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 71194-27:
(7*7)+(6*1)+(5*1)+(4*9)+(3*4)+(2*2)+(1*7)=119
119 % 10 = 9
So 71194-27-9 is a valid CAS Registry Number.

71194-27-9SDS

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 methyl 10-chloroundecanoate

1.2 Other means of identification

Product number -
Other names methyl 10-chlorodecanoate

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:71194-27-9 SDS

71194-27-9Upstream product

71194-27-9Relevant articles and documents

METATHESIS REACTIONS OF UNSATURATED ESTERS CATALYZED BY HOMOGENEOUS TUNGSTEN COMPLEXES. SYNTHESES OF CIVETONE AND MACROLIDES

Tsuji, Jiro,Hashiguchi, Shohei

, p. 69 - 80 (1981)

The metathesis reactions of methyl 10-undecenoate, methyl oleate and oleyl acetate have been carried out using WCl6 and WOCl4 as primary catalysts and SnMe4, PbMe4, Cp2TiMe2, and Cp2ZrMe2 as cocatalysts.The catalyst system WOCl4/Cp2TiMe2 was found to be very active for the metathesis of the unsaturated esters and is somewhat better than the system WCl6/SnMe4.Diethyl 9-octadecene-1,18-dioate, obtained by the metathesis of ethyl oleate, was subjected to the Dieckmann cyclization.The cyclized product was decarboxylated to give civetone as a mixture of the cis and trans isomers.Preliminary studies of macrolide synthesis by the intramolecular metathesis of oleyl oleate and 10-undecenyl 10-undecenoate to afford 9-octadecen-18-olide and 10-eicosen-20-olide, respectively, have been carried out.

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