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Propanedioic acid, [4-(acetyloxy)-2-cyclohexen-1-yl]-, dimethyl ester, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82736-53-6

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82736-53-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82736-53-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,7,3 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 82736-53:
(7*8)+(6*2)+(5*7)+(4*3)+(3*6)+(2*5)+(1*3)=146
146 % 10 = 6
So 82736-53-6 is a valid CAS Registry Number.

82736-53-6SDS

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 dimethyl (trans-4-acetoxycyclohex-2-en-1-yl)malonate

1.2 Other means of identification

Product number -
Other names dimethyl trans-4-acetoxy-2-cyclohexenylmalonate

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:82736-53-6 SDS

82736-53-6Relevant academic research and scientific papers

Palladium-catalyzed substitution of allylic fluorides

Hazari, Amaruka,Gouverneur, Ve,Brown, John M.

supporting information; body text, p. 1296 - 1299 (2009/06/30)

As unusual substrates for the Tsuji-Trost allylation reaction, allylic fluorides are responsive to palladiumcatalyzed substitution. Their activity towards this reaction fits in the series OCO2Me>OBz? F? OAc. The classic stereoretention mechanis

Stereoselective Synthesis of Vinylcyclopropanes via Palladium-Catalyzed Reactions

Baeckvall, J. E.,Vagberg, J. O.,Zercher, C.,Genet, J. P.,Denis, A.

, p. 5430 - 5435 (2007/10/02)

Vinylcyclopropanes were synthesized in a stereocontrolled manner from 1-acetoxy-4-chloro-2-alkenes.A stereospecific palladium-catalyzed substitution of the chloro group by dimethyl malonate anion and subsequent palladium-catalyzed cyclization afforded the

STEREOSPECIFIC PALLADIUM-CATALYZED 1,4-ACETOXYCHLORINATION OF 1,3-DIENES

Baeckvall, Jan-E.,Nordberg, Ruth E.,Nystroem, Jan-E.

, p. 1617 - 1620 (2007/10/02)

Palladium-catalyzed oxidation of 1,3-dienes in acetic acid in the presence of LiCl and LiOAc produces 1-acetoxy-4-chloro-2-alkenes in high selectivity.The 1,4-adducts were stereo- and regioselectively functionalized.

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