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7-Cyclotetradecene-1-carboxylic acid, 7,11-dimethyl-4-(1-methylethyl)-3,13-dioxo-2-[(R)-phenylsulfinyl]-, methyl ester, (1R,2S,4S,7E,11S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

646519-72-4

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646519-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 646519-72-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,6,5,1 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 646519-72:
(8*6)+(7*4)+(6*6)+(5*5)+(4*1)+(3*9)+(2*7)+(1*2)=184
184 % 10 = 4
So 646519-72-4 is a valid CAS Registry Number.

646519-72-4SDS

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 (E)-(1R,2S,4S,11S)-2-((R)-Benzenesulfinyl)-4-isopropyl-7,11-dimethyl-3,13-dioxo-cyclotetradec-7-enecarboxylic acid methyl ester

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:646519-72-4 SDS

646519-72-4Downstream Products

646519-72-4Relevant academic research and scientific papers

Pyranophane Transannular Diels-Alder Approach to (+)-Chatancin: A Biomimetic Asymmetric Total Synthesis

Soucy, Pierre,L'Heureux, Alexandre,Toro, Andras,Deslongchamps, Pierre

, p. 9983 - 9987 (2007/10/03)

An asymmetric total synthesis of (+)-chatancin was achieved via a transannular Diels-Alder (TADA) reaction of an in situ generated macrocyclic pyranophane pseudobase. The presented route constitutes the second of two proposed biosynthetic pathways that in

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