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183022-61-9

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183022-61-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183022-61-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,0,2 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 183022-61:
(8*1)+(7*8)+(6*3)+(5*0)+(4*2)+(3*2)+(2*6)+(1*1)=109
109 % 10 = 9
So 183022-61-9 is a valid CAS Registry Number.

183022-61-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethynyl-4-[2-(4-nitrophenyl)ethynyl]benzene

1.2 Other means of identification

Product number -
Other names 4,4'-HCCC6H4CCC6H4NO2

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:183022-61-9 SDS

183022-61-9Relevant articles and documents

Synthesis, characterization and DFT calculations of new ethynyl-bridged C60 derivatives

Rondeau-Gagné, Simon,Curutchet, Carles,Grenier, Fran?ois,Scholes, Gregory D.,Morin, Jean-Fran?ois

experimental part, p. 4230 - 4242 (2010/07/08)

A new series of soluble C60 derivatives for organic electronic application has been synthesized by ethynylation reaction using different electron-donating and electron-withdrawing groups of varying length.

Selective and efficient access to ortho, meta and para ring-substituted phenylacetylene derivatives R-[C≡C-C6H4](x)-Y (Y:H, NO2, CN, I, NH2)

Lavastre, Olivier,Cabioch, Sandrine,Dixneuf, Pierre H.,Vohlidal, Jiri

, p. 7595 - 7604 (2007/10/03)

ortho, meta and para isomers of iodo and amino ring-substituted phenylacetylene as well as rod-like arylacetylene derivatives were prepared by a simple synthetic route involving three consecutive reactions: the palladium-catalysed carbon-carbon bond forma

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