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2-(4-nitrophenyl)-1,3-oxazolidine is a chemical compound characterized by its molecular formula C9H9NO3. It is a derivative of oxazolidine with a nitrophenyl group attached to one of its carbon atoms, forming a five-membered oxazolidine ring. 2-(4-nitrophenyl)-1,3-oxazolidine is recognized for its potential as a chiral building block in the synthesis of biologically active molecules and pharmaceuticals, and it may also possess unique properties that could be valuable in various chemical and pharmaceutical applications.

82191-80-8

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82191-80-8 Usage

Uses

Used in Organic Synthesis:
2-(4-nitrophenyl)-1,3-oxazolidine is utilized as a chiral building block in organic synthesis for the preparation of various biologically active molecules. Its unique structure allows for the creation of complex organic compounds that can be used in a wide range of applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-(4-nitrophenyl)-1,3-oxazolidine is employed as a key intermediate in the development of new drugs. Its chiral properties make it a valuable component in the synthesis of pharmaceuticals with specific therapeutic effects.
Used in Chemical Research:
2-(4-nitrophenyl)-1,3-oxazolidine's potential interesting properties also make it a candidate for further chemical research, where it could be explored for new applications or to enhance existing chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 82191-80-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,9 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82191-80:
(7*8)+(6*2)+(5*1)+(4*9)+(3*1)+(2*8)+(1*0)=128
128 % 10 = 8
So 82191-80-8 is a valid CAS Registry Number.

82191-80-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-nitrophenyl)-1,3-oxazolidine

1.2 Other means of identification

Product number -
Other names 2-(4-nitro-phenyl)-oxazolidine

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:82191-80-8 SDS

82191-80-8Relevant academic research and scientific papers

Efficient oxidative conversion of aldehydes to 2-substituted oxazolines and oxazines using (diacetoxyiodo)benzene

Karade, Nandkishor N.,Tiwari, Girdharilal B.,Gampawar, Sumit V.

, p. 1921 - 1924 (2008/03/27)

An efficient synthesis of 2-substituted oxazolines from aldehydes and 2-amino alcohol using (diacetoxyiodo)benzene as an oxidant, is reported. (Diacetoxyiodo)benzene acts as a mild dehydrogenating agent to convert the initially formed oxazolidine from ald

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