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13719-82-9

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13719-82-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13719-82-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,1 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13719-82:
(7*1)+(6*3)+(5*7)+(4*1)+(3*9)+(2*8)+(1*2)=109
109 % 10 = 9
So 13719-82-9 is a valid CAS Registry Number.

13719-82-9SDS

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 1,2-Bis(bromomethyl)-3,4,5,6-tetrafluorobenzene

1.2 Other means of identification

Product number -
Other names 1,2-bis-bromomethyl-3,4,5,6-tetrahydrofluorobenzene

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:13719-82-9 SDS

13719-82-9Relevant articles and documents

Synthesis and characterization of electron-deficient pentacenes

Swartz, Christopher R.,Parkin, Sean R.,Bullock, Joseph E.,Anthony, John E.,Mayer, Alex C.,Malliaras, George G.

, p. 3163 - 3166 (2005)

(Chemical Equation Presented) Halogen functional groups on pentacene can be used both as synthetic handles for further functionalization as well as to tune the π-stacking in these systems. The halogenated pentacene derivatives described here (X = Br, X′ =

Diversity oriented approach to polycyclic compounds through the diels-alder reaction and the Suzuki coupling

Kotha, Sambasivarao,Misra, Shilpi,Srinivas, Venu

, p. 4052 - 4062 (2012/09/07)

A diversity oriented strategy has been demonstrated to deliver small "drug like" molecules using alkylation, Diels-Alder reaction, and Suzuki-Miyaura cross-coupling as key steps. This methodology allows access a wide range of molecules using simple scaffolds such as indanes, tetralins and tetrahydroisoquinolines, which can enhance the chemical space for potential therapeutic molecules.

Isoindolinyl derivatives

-

, (2008/06/13)

Esters of lower alkanoic acids substituted at the α-position with isoindoline or tetrahydroisoquinoline, and intermediates therefor, useful as pesticides.

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