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Diazenecarbonitrile, (4-chlorophenyl)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20750-84-9

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20750-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20750-84-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,7,5 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 20750-84:
(7*2)+(6*0)+(5*7)+(4*5)+(3*0)+(2*8)+(1*4)=89
89 % 10 = 9
So 20750-84-9 is a valid CAS Registry Number.

20750-84-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-(4-chloro-phenyl)-diazenecarbonitrile

1.2 Other means of identification

Product number -
Other names 4-chlorobenzenediazocyanide

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:20750-84-9 SDS

20750-84-9Relevant academic research and scientific papers

OXIDATIVE FRAGMENTATION OF 3-ARYL-1-(TETRAZOL-5'-YL)TRIAZENES: A NEW ROUTE TO ARYL DIAZOCYANIDES.

Butler, Richard N.,Shelly, Declan P.

, p. 3401 - 3402 (1985)

Oxydation of 3-aryl-1-(tetrazol-5'-yl)triazenes with Pb(OAc)4 resulted in a fragmentation and gave aryldiazocyanides.

Reaction of 3-Aryl-1-(tetrazol-5'-yl)triazines with some Electrophiles: Mercury Derivatives and Fragmentations: A New Route to Aryl Diazocyanides

Butler, Richard N.,Shelly, Declan P.

, p. 1101 - 1106 (2007/10/02)

Treatment of 3-aryl-1-(tetrazol-5'-yl)triazines (4) with lead tetra-acetate resulted in a fragmentation to aryl-diazocyanides.The triazines (4) and their monomethyl derivatives when treated with mercuric acetate and phenylmercury hydroxide gave stable mer

Phase-Transfer Synthesis of Arenediazocyanides and Synthesis of Arenediazosulfones from Arenediazonium Cations and the Formation of Reduced Pyridazines by 2 + 4 Cycloaddition Reactions

Ahern, Michael F.,Leopold, Ahuva,Beadle, James R.,Gokel, George W.

, p. 548 - 554 (2007/10/02)

The remarkably versatile arenediazonium cations are also convenient to use and nondangerous when utilized as the BF4 or PF6 salts.Arenediazonium compounds have recently been shown to undergo the 2 + 4 Diels-Alder cycloaddition, but the reaction is solvent

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