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5633-36-3

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5633-36-3 Usage

Description

[3-(4-nitrophenyl)oxiran-2-yl](phenyl)methanone, also known as nitrophenylpropiophenone epoxide, is an organic compound with the molecular formula C15H11NO4. It is an epoxide derivative featuring a phenyl ring connected to an oxirane ring with a nitro group and a ketone group. [3-(4-nitrophenyl)oxiran-2-yl](phenyl)methanone is recognized for its versatile chemical properties, making it a valuable precursor in the synthesis of pharmaceuticals and other organic compounds.

Uses

Used in Pharmaceutical Synthesis:
[3-(4-nitrophenyl)oxiran-2-yl](phenyl)methanone is used as a precursor in the pharmaceutical industry for the synthesis of various drugs. Its unique structure and reactivity allow for the creation of a wide range of medicinal compounds, contributing to the development of novel treatments for different health conditions.
Used in Organic Chemistry Research:
In the field of organic chemistry, [3-(4-nitrophenyl)oxiran-2-yl](phenyl)methanone serves as a key intermediate for the synthesis of complex organic molecules. Its epoxide and nitro group functionalities enable it to participate in various chemical reactions, such as ring-opening and reduction, making it a valuable tool for researchers in organic chemistry.
Used in Chemical Intermediates Production:
[3-(4-nitrophenyl)oxiran-2-yl](phenyl)methanone is also utilized as a chemical intermediate in the production of other organic compounds. Its ability to undergo various chemical transformations makes it a useful building block for creating a diverse array of molecules with potential applications in different industries, such as agriculture, materials science, and the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 5633-36-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,3 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5633-36:
(6*5)+(5*6)+(4*3)+(3*3)+(2*3)+(1*6)=93
93 % 10 = 3
So 5633-36-3 is a valid CAS Registry Number.

5633-36-3SDS

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 [3-(4-nitrophenyl)oxiran-2-yl]-phenylmethanone

1.2 Other means of identification

Product number -
Other names 3-Methylamino-1-(4-methoxy-phenyl)-propan

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:5633-36-3 SDS

5633-36-3Relevant articles and documents

Pyrenediones as versatile photocatalysts for oxygenation reactions with: In situ generation of hydrogen peroxide under visible light

Zhang, Yuannian,Yang, Xin,Tang, Haidi,Liang, Dong,Wu, Jie,Huang, Dejian

supporting information, p. 22 - 27 (2020/01/13)

Pyrenediones (PYDs) are efficient photocatalysts for three oxygenation reactions: Epoxidation of electron deficient olefins, oxidative hydroxylation of organoborons, and oxidation of sulfides via in situ generation of H2O2 under visible light irradiation, using oxygen as a terminal oxidant and IPA as a solvent and a hydrogen donor.

Facile epoxidation of α, β-unsaturated ketones with urea-2,2-dihydroperoxypropane as a new oxidant

Khosravi, Kaveh,Naserifar, Shirin

, p. 323 - 328 (2017/01/10)

Abstract: Various aromatic α, β-unsaturated ketones were successfully transformed into their corresponding epoxides using urea-2,2-dihydroperoxypropane as the oxygen source for the first time. The reactions were carried out under mild alkaline conditions at room temperature in high yields and short reaction times. Graphical Abstract: [Figure not available: see fulltext.]

A highly enantioselective asymmetric Darzens reaction catalysed by proline based efficient organocatalysts for the synthesis of di- and tri-substituted epoxides

Ashokkumar, Veeramanoharan,Siva, Ayyanar,Ramaswamy Chidambaram

supporting information, p. 10926 - 10929 (2017/10/13)

A new class of easily available and readily tunable proline based chiral organocatalysts was found to efficiently catalyse an unprecedented highly enantioselective asymmetric Darzens reaction of α-chloroketones and substituted α-chloroketones with various

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