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1264712-19-7

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1264712-19-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1264712-19-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,4,7,1 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1264712-19:
(9*1)+(8*2)+(7*6)+(6*4)+(5*7)+(4*1)+(3*2)+(2*1)+(1*9)=147
147 % 10 = 7
So 1264712-19-7 is a valid CAS Registry Number.

1264712-19-7SDS

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 3-[1-(2-fluorophenyl)naphthalen-2-ylsulfanyl]propionic acid ethyl 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:1264712-19-7 SDS

1264712-19-7Downstream Products

1264712-19-7Relevant articles and documents

Synthesis of functionalized dibenzothiophenes- An efficient three-step approach based on Pd-catalyzed C-C and C-S bond formations

Jepsen, Tue Heesgaard,Larsen, Mogens,Jorgensen, Morten,Solanko, Katarzyna A.,Bond, Andrew D.,Kadziola, Anders,Nielsen, Mogens Brondsted

, p. 53 - 57 (2011/03/21)

A novel and efficient three-step protocol for synthesizing functionalized dibenzothiophenes (DBTs) from common starting materials and by using palladium-catalyzed carbon-carbon and carbon-sulfur bond formations is presented. The reaction conditions offer significantly improved functional-group tolerance and regioselectivity as compared to previously reported methods. A flexible and concise three-step protocol for the synthesis of functionalized dibenzothiophenes DBTs from readily available starting materials is presented. The method is based on two palladium-catalyzed reactions to prepare the masked thiophenols 4followed by deprotection and in situ cyclization to form the DBT skeleton. This approach offers improved functional-group tolerance as well as regiocontrol in the synthesis of functionalized DBTs as compared to previously reported methods.

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