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65000-79-5

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65000-79-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65000-79-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,0,0 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65000-79:
(7*6)+(6*5)+(5*0)+(4*0)+(3*0)+(2*7)+(1*9)=95
95 % 10 = 5
So 65000-79-5 is a valid CAS Registry Number.

65000-79-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-acetamido-4-diethylamino-6-diethylphosphonato-2',4'-dinitroazobenzene

1.2 Other means of identification

Product number -
Other names Diethyl-3,5-dinitro-6-<2-acetylamino-4-(N,N-diethylamino)-phenylazo>-phenylphosphonat

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:65000-79-5 SDS

65000-79-5Downstream Products

65000-79-5Relevant articles and documents

Phosphonation of Aryl Halides by Copper(I) Complexes of Trialkyl Phosphites

Connor, Joseph A.,Dubowski, Danuta,Jones, Anthony,Price, Raymond

, p. 1143 - 1148 (2007/10/02)

The copper complexes 2> (1; R=Me or Et), (bpy)> (2; R=Me or Et) (bpy is 2,2'-bipyridine), and 2> react with certain 2-halogenoazobenzene compounds, ArX, at room temperature to form the corresponding dialkyl arylphosphonates, ArP(O)(OR)2, and the products, ArH and Ar2, of reductive substitution and biaryl coupling.The ester, MeCO2R, and a copper(I) halide complex (e.g. >) are also formed.Kinetic studies of the reactions of some of these copper complexes with 2'-acetamido-6-bromo-4'-diethylamino-2,4-dinitroazobenzene in alcohol solution show that the phosphonation reactions are equal concentration second-order processes in each case.The effects of a radical scavenger and of light on the reaction suggest the involvement of radicals in the formation of ArH and Ar2, but not in the formation of ArP(O)(OR)2.The effects of different substituents in ArX, of changes in solvent, and of various additives on these reactions are investigated.A mechanism involving concerted nucleophilic substitution within the coordination sphere of copper(I) is proposed.

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