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Propanoic acid, 2,2-dimethyl-, [1-[2-[(1S)-1-methyl-3-(1-methylethyl)-2-[[(trifluoromethyl)sulfonyl]oxy]-2- cyclopenten-1-yl]ethyl]-4-oxo-2,5-cyclohexadien-1-yl]methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

868615-41-2

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868615-41-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 868615-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,6,1 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 868615-41:
(8*8)+(7*6)+(6*8)+(5*6)+(4*1)+(3*5)+(2*4)+(1*1)=212
212 % 10 = 2
So 868615-41-2 is a valid CAS Registry Number.

868615-41-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S)-{1-[2-(3-isopropyl-1-methyl-2-{[(trifluoromethyl)sulfonyl]oxy}cyclopent-2-en-1-yl)ethyl]-4-oxocyclohexa-2,5-dien-1-yl}methyl 2,2-dimethylpropanoate

1.2 Other means of identification

Product number -
Other names 2,2-Dimethyl-propionic acid 1-[2-((S)-3-isopropyl-1-methyl-2-trifluoromethanesulfonyloxy-cyclopent-2-enyl)-ethyl]-4-oxo-cyclohexa-2,5-dienylmethyl ester

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:868615-41-2 SDS

868615-41-2Downstream Products

868615-41-2Relevant academic research and scientific papers

Synthetic studies on cyathin terpenoids: Enantioselective synthesis of the tricyclic core of cyathin through intramolecular Heck cyclisation

Drege, Emmanuelle,Tominiaux, Cyrille,Morgant, Georges,Desmaele, Didier

, p. 4825 - 4840 (2007/10/03)

An enantioselective synthesis of the tricyclic ketone (+)-5, which displays the carbon core of NGF-inducing cyathane diterpenes, has been completed according to a strategy in which the key step was the intramolecular Heck reaction of the AC subunit 49 est

Asymmetric synthesis of the tricyclic core of cyathin diterpenoids via intramolecular Heck reaction

Drège, Emmanuelle,Morgant, Georges,Desma?le, Didier

, p. 7263 - 7266 (2007/10/03)

The enantioselective synthesis of the ketones 3 which displays the carbon core of NGF-inducing cyathane diterpenes is described. The key tricyclic trienone 22 was assembled in 13 steps from Michael adduct (R)-8a via intramolecular Heck cyclization of the

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