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1,4-Benzenediamine, N,N'-bis(2-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

47500-72-1

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47500-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 47500-72-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,7,5,0 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 47500-72:
(7*4)+(6*7)+(5*5)+(4*0)+(3*0)+(2*7)+(1*2)=111
111 % 10 = 1
So 47500-72-1 is a valid CAS Registry Number.

47500-72-1SDS

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 1-N,4-N-bis(2-nitrophenyl)benzene-1,4-diamine

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:47500-72-1 SDS

47500-72-1Relevant academic research and scientific papers

High-Pressure Synthesis of Oligoanilines

Brown, Christopher L.,Muderawan, I. Wayan,Young, David J.

, p. 2511 - 2517 (2003)

Aniline oligomers can be prepared cleanly and in high yield by the high-pressure promoted SNAr reaction of aromatic amines with fluoronitrobenzenes followed by reduction of the nitro group.

Syntheses and Reactivity of Bisflavins. Oxidation of N-Benzyl-1,4-dihydronicotinamide by Flavins in Aqueous Solution

Yano, Yumihiko,Ohya, Eiichi

, p. 1227 - 1232 (2007/10/02)

Several bisflavins linked at the 10,10'-positions of isoalloxazine rings have been synthesized.The kinetics of the oxidation of N-benzyl-1,4-dihydronicotinamide in aqueous solution have been examined.It has been found that each flavin of a bisflavin is considerably influenced by another intramolecular flavin moiety due to the formation of a charge-transfer complex between intramolecularly reduced and oxidized flavins.The formation of the complex depends on the conformation.

UNUSUAL KINETIC BEHAVIOR OF BIS-FLAVIN FOR N-BENZYL-1,4-DIHYDRONICOTINAMIDE (BNAH) REDUCTION IN AN AQUEOUS SOLUTION

Yano, Yumihiko,Ohya, Eiichi

, p. 1281 - 1284 (2007/10/02)

Several bis-flavins linked at 10,10'-positions of isoalloxazine rings were synthesized.The reactivity of each flavin of a bis-flavin was found to be considerably influenced by another intramolecular flavin moiety, depending on the conformation of the bis-

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