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trans-2-iodocyclohexyl propynoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

115377-01-0

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115377-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115377-01-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,3,7 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 115377-01:
(8*1)+(7*1)+(6*5)+(5*3)+(4*7)+(3*7)+(2*0)+(1*1)=110
110 % 10 = 0
So 115377-01-0 is a valid CAS Registry Number.

115377-01-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-2-iodocyclohexyl propynoate

1.2 Other means of identification

Product number -
Other names -

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:115377-01-0 SDS

115377-01-0Relevant academic research and scientific papers

Synthesis of iodoalkylidene lactones from alkenes

Haaima,Lynch,Routledge,Weavers

, p. 4229 - 4252 (1993)

Alkenes are reality transformed into iodo acetylenic esters by addition of acetylenic acids in the presence of a source of iodonium ion. A subsequent free-radical cyclisation induced by dibenzoyl peroxide leads to (E)-iodoalkylidene butyrolactones.

IODOVINYLIDENE LACTONE SYNTHESIS. FREE RADICAL CYCLISATION OF IODO ACETYLENIC ESTERS.

Haaima, Gerald,Weavers, Rex T.

, p. 1085 - 1088 (2007/10/02)

Propiolic acids add to alkenes in the presence of N-iodosuccinimide to give iodo acetylenic esters.These, on treatment with dibenzoyl peroxide, undergo cyclisation to yield (E)-iodovinylidene butyrolactones.Subsequent alkylation with lithium dimethylcuprate occurs by replacement of the iodine.

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