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2,2'-DiMethoxy-5,5'-dinitro-1,1'-biphenyl is a chemical compound that is an analog of p-acetamidopheno (A161220). It is characterized by the presence of two methoxy groups and two nitro groups attached to a biphenyl core.

81763-59-9

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81763-59-9 Usage

Uses

Used in Enzyme Activity Assays:
2,2'-DiMethoxy-5,5'-dinitro-1,1'-biphenyl is used as a substrate for determining peroxidase activities. It serves as a valuable tool in the study and analysis of peroxidase enzymes, which play a crucial role in various biological processes.
Used in Pharmaceutical Research:
As an analog of p-acetamidopheno, 2,2'-DiMethoxy-5,5'-dinitro-1,1'-biphenyl may have potential applications in pharmaceutical research, particularly in the development of new drugs and therapies. Its unique structure and properties could contribute to the discovery of novel compounds with therapeutic potential.
Used in Chemical Synthesis:
2,2'-DiMethoxy-5,5'-dinitro-1,1'-biphenyl can also be utilized in chemical synthesis processes, where it may serve as a building block or intermediate for the production of other complex organic compounds. Its versatility in chemical reactions could make it a valuable component in the synthesis of various molecules with diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 81763-59-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,7,6 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81763-59:
(7*8)+(6*1)+(5*7)+(4*6)+(3*3)+(2*5)+(1*9)=149
149 % 10 = 9
So 81763-59-9 is a valid CAS Registry Number.

81763-59-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2'-dimethoxy-5,5'-dinitrobiphenyl

1.2 Other means of identification

Product number -
Other names 5.5'-dinitro-2.2'-dimethoxy-diphenyl

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:81763-59-9 SDS

81763-59-9Relevant academic research and scientific papers

Gold-catalyzed direct oxidative coupling reactions of non-activated arenes

Kar, Anirban,Mangu, Naveenkumar,Kaiser, Hanns Martin,Tse, Man Kin

experimental part, p. 524 - 537 (2009/06/05)

A general gold-catalyzed oxidative homo- and hetero-coupling of arenes in mild conditions is described. This reaction gives moderate to excellent yield using PhI(OAc)2 as an oxidant. The effects of temperature, solvent, oxidant and concentration of substrate in this process have also been studied in detail. The product identity and distribution as well as the substrate limitation give us insights into this type of gold catalysts. Depending upon the reaction conditions, the gold catalyst behaves as a simple Lewis acid, which produces amines from arenes using DIAD as an aminating reagent.

A general gold-catalyzed direct oxidative coupling of non-activated arenes

Kar, Anirban,Mangu, Naveenkumar,Kaiser, Hanns Martin,Beller, Matthias,Tse, Man Kin

, p. 386 - 388 (2008/09/18)

A gold-catalyzed mild and general oxidative homo-coupling of arenes using PhI(OAc)2 as the oxidant is described (13 examples, 31-81% yield). The Royal Society of Chemistry.

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