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83626-78-2

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83626-78-2 Usage

Chemical compound

2-6-[6-(1-Oxo-1,3-dihydro-isoindol-2-yl)-hexyldisulfanyl]-hexyl-isoindole-1,3-dione

Class

Isoindole-1,3-dione derivative

Structure

Central isoindole-1,3-dione ring with two side chains

Side chains

Hexyldisulfanyl group
1-oxo-1,3-dihydro-isoindol-2-yl group

Potential applications

Pharmaceuticals and organic synthesis

Unique structure

May exhibit interesting biological activities

Uses

Building block for synthesis of complex molecules

Further research

Needed for full understanding of properties and uses.

Check Digit Verification of cas no

The CAS Registry Mumber 83626-78-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,6,2 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 83626-78:
(7*8)+(6*3)+(5*6)+(4*2)+(3*6)+(2*7)+(1*8)=152
152 % 10 = 2
So 83626-78-2 is a valid CAS Registry Number.

83626-78-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[6-[6-(3-oxo-1H-isoindol-2-yl)hexyldisulfanyl]hexyl]isoindole-1,3-dione

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:83626-78-2 SDS

83626-78-2Relevant articles and documents

New organic picolylamine-type ligands and electrochemical study of their complexation with Cu(MeCN)4ClO4

Majouga,Romashkina,Kashaev,Beloglazkina,Moiseeva,Zyk

, p. 261 - 268 (2011/11/05)

A series of novel organic ligands with dipicolylamine and disulfide groups connected by polymethylene, alkylaryl, alkoxyaryl, or alkoxycarbonyl linker was synthesized. The electrochemical study by cyclic voltammetry was carried out for two synthesized lig

Synthesis of ω-(4-aminophenylsulfonamido)alkyl disulfides and thiosulfates and their activity against dihydropteroate synthetase from sulfanilamide-resistant Neisseria gonorrhoeae

Foye,Kauffman,Suttimool

, p. 799 - 802 (2007/10/02)

A series of ω-(4-aminophenylsulfonamido)alkyl disulfides and ω-(4-aminophenylsulfonamido)alkanethiosulfates was synthesized from the reaction of p-acetamidobenzenesulfanilyl chloride and either the aminoalkyl disulfide dihydrobromide or the aminoalkyl bro

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