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(o-Nitrophenyl)-p-benzoquinone is a dark brown solid that serves as a reactant in the synthesis of monoaryl-p-benzoquinones, which are a class of organic compounds with various applications in chemical and pharmaceutical industries.

105946-79-0

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105946-79-0 Usage

Uses

Used in Chemical Synthesis:
(o-Nitrophenyl)-p-benzoquinone is used as a reactant for the preparation of monoaryl-p-benzoquinones, which are important intermediates in the synthesis of various organic compounds.
Used in Pharmaceutical Industry:
(o-Nitrophenyl)-p-benzoquinone is used as a reactant in the synthesis of pharmaceutical compounds, contributing to the development of new drugs and therapeutic agents.
Used in Research and Development:
(o-Nitrophenyl)-p-benzoquinone is utilized in research and development for studying the properties and reactions of monoaryl-p-benzoquinones, aiding in the advancement of scientific knowledge and innovation in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 105946-79-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,9,4 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 105946-79:
(8*1)+(7*0)+(6*5)+(5*9)+(4*4)+(3*6)+(2*7)+(1*9)=140
140 % 10 = 0
So 105946-79-0 is a valid CAS Registry Number.

105946-79-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-nitro-phenyl)-[1,4]benzoquinone

1.2 Other means of identification

Product number -
Other names (2-Nitro-phenyl)-[1,4]benzochinon

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:105946-79-0 SDS

105946-79-0Relevant academic research and scientific papers

C-H arylation reactions through aniline activation catalysed by a PANI-g-C3N4-TiO2 composite under visible light in aqueous medium

Wang, Liang,Shen, Jun,Yang, Sen,Liu, Wenjie,Chen, Qun,He, Mingyang

, p. 1290 - 1296 (2018)

A PANI (polyaniline)-g-C3N4-TiO2 composite was prepared and found to be efficient for radical C-H arylation reactions. The arylation process involved coupling of in situ generated aryl diazonium salts from aniline with heteroarenes, enol acetates or benzoquinones under visible light in aqueous medium or pure water. A broad range of substrates survived the reaction conditions to provide the desired products in moderate to good yields. Scale-up (10 mmol) synthesis was also achieved. This semiconductor photocatalyst showed good photocatalytic performance and stability. Recycle studies showed that this composite could be readily recovered and a slight decrease in the catalytic activity was observed after ten consecutive runs.

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