OXAZOLIDINE

Investigational

Details

Stereochemistry	ACHIRAL
Molecular Formula	C3H7NO
Molecular Weight	73.0938
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

SMILES

C1COCN1

InChI

InChIKey=WYNCHZVNFNFDNH-UHFFFAOYSA-N

InChI=1S/C3H7NO/c1-2-5-3-4-1/h4H,1-3H2

HIDE SMILES / InChI

Description

Oxazolidine molecule consists of three carbons, nitrogen, and oxygen. Oxazolidines is a key molecular moiety in biologically active compounds. Some derivatives, the oxazolidinediones, are used as anticonvulsants.

Approval Year

PubMed

Show entries

Title	Date	PubMed
Diastereoselective epoxidation of oxazolidine-substituted alkenes by dimethyldioxirane and m-chloroperbenzoic acid: pi-facial control through hydrogen bonding by the urea functionality.	2001 Jan 11	11429877
Three-dimensional common-feature hypotheses of inhibitors of calling behaviour and in vitro [14C]acetate incorporation by pheromone glands of Plodia interpunctella.	2002 Nov	12449530
First asymmetric synthesis of 6-hydroxy-4-sphingenine-containing ceramides. Use of chiral propargylic alcohols to prepare a lipid found in human skin.	2003 Jan 24	12530859
Enantioselective indole Friedel--Crafts alkylations catalyzed by bis(oxazolinyl)pyridine-scandium(III) triflate complexes.	2003 Sep 10	12952445
Effects of KST48 [(2R,5SR)3-(2-chlorobenzoyl)-5-(4-chlorophenoxymethyl)-2(3,4-dichlorophenyl) oxazolidine] on glucose transport in L6 myocytes.	2004	15646367

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Patents

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Name

Type

Language

OXAZOLIDINE

Preferred Name

English

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Code System

Code

Type

Description

WIKIPEDIA

OXAZOLIDINE

PRIMARY

FDA UNII

13F52UF6MR

PRIMARY

PUBCHEM

536683

PRIMARY

EPA CompTox

DTXSID50198446

PRIMARY

CHEBI

38330

PRIMARY

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SUBSTANCE RECORD


					13F52UF6MR

OXAZOLIDINE

SMILES

InChI

Description<div class="info-popup-container"><div><span class="pop-sub-key ">Sources:&nbsp;</span><span class="pop-sub-val"><span class="ext-link"><a target="_self" href="https://www.ncbi.nlm.nih.gov/pubmed/22466369">https://www.ncbi.nlm.nih.gov/pubmed/22466369</a></span></span></div></div>

Approval Year

PubMed

Patents

Description