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Methanone, (4-hydroxyphenyl)(3-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72090-63-2

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72090-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72090-63-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,0,9 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 72090-63:
(7*7)+(6*2)+(5*0)+(4*9)+(3*0)+(2*6)+(1*3)=112
112 % 10 = 2
So 72090-63-2 is a valid CAS Registry Number.

72090-63-2SDS

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 m-NHB

1.2 Other means of identification

Product number -
Other names (4-Hydroxy-phenyl)-(3-nitro-phenyl)-methanone

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:72090-63-2 SDS

72090-63-2Relevant academic research and scientific papers

PHOTOACTIVATABLE FOULING-RESISTANT COPOLYMERS

-

, (2017/03/14)

A photoactivatable fouling-resistant copolymer composed of a photoactivatable monomer and a hydrophilic monomer is disclosed. The photoactivatable monomer includes an aryl ketone derivative having one or more polar groups or alkyl groups.

Visible Light Copper Photoredox-Catalyzed Aerobic Oxidative Coupling of Phenols and Terminal Alkynes: Regioselective Synthesis of Functionalized Ketones via C C Triple Bond Cleavage

Sagadevan, Arunachalam,Charpe, Vaibhav Pramod,Ragupathi, Ayyakkannu,Hwang, Kuo Chu

supporting information, p. 2896 - 2899 (2017/03/11)

Direct oxidative coupling of phenols and terminal alkynes was achieved at room temperature by a visible-light-mediated copper-catalyzed photoredox process. This method allows regioselective synthesis of hydroxyl-functionalized aryl and alkyl ketones from simple phenols and phenylacetylene via C C triple bond cleavage. 47 examples were presented. From a synthetic perspective, this protocol offers an efficient synthetic route for the preparation of pharmaceutical drugs, such as pitofenone and fenofibrate.

Synthesis and characterization of fluorinated polyimides derived from novel unsymmetrical diamines

Yang, Fengchun,Li, Yanfeng,Ma, Tao,Bu, Qianqian,Zhang, Shujiang

experimental part, p. 767 - 775 (2010/09/04)

Two kinds of aromatic, unsymmetrical diamines with ether-ketone group, 3-amino-4'-(4-amino-2- trifluoromethylphenoxy)-benzophenone and 4-amino-4'-(4-amino-2-trifluoromethylphenoxy)-benzophenone, were successfully synthesized with two different synthetic r

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