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857591-68-5

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857591-68-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 857591-68-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,7,5,9 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 857591-68:
(8*8)+(7*5)+(6*7)+(5*5)+(4*9)+(3*1)+(2*6)+(1*8)=225
225 % 10 = 5
So 857591-68-5 is a valid CAS Registry Number.

857591-68-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-aminophenyl)selanylaniline

1.2 Other means of identification

Product number -
Other names Benzenamine,2,2'-selenobis

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:857591-68-5 SDS

857591-68-5Downstream Products

857591-68-5Relevant articles and documents

Bis(2-nitrophenyl) selenide, bis(2-aminophenyl) selenide and bis(2-aminophenyl) telluride: Structural and theoretical analysis

Butcher, Ray J.,Saravanan, Raju,Singh, Harkesh B.

, p. 271 - 280 (2021/06/14)

Three organoselenium and organotellurium compounds containing ortho substitutents, namely, bis(2-nitrophenyl) selenide, C12H8N2O4Se, 2, bis(2-aminophenyl) selenide, C12H12N2Se, 3, and bis(2-aminophenyl) telluride, C12H12N2Te, 7, have been investigated by

Microwave-assisted Cu2O-catalyzed one-pot synthesis of symmetrical diaryl selenides from elemental selenium

Zhang, Shaozhong,Karra, Kranthi,Heintz, Christina,Kleckler, Erica,Jin, Jin

supporting information, p. 4753 - 4755 (2013/08/23)

A novel and simple microwave-assisted one-pot protocol to prepare symmetrical diaryl selenides has been developed. A cross-coupling reaction between aryl iodide and elemental selenium takes place in the presence of KOH and a catalytic amount of Cu2O/NH2CH2CH 2NH2, leading to C-Se bond formation. The reactions are highly efficient with a reaction time of 1 h under microwave irradiation and yields from 50% to 90%.

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