(S)-(-)-4-Isopropyl-2-oxazolidinone, 98%

Name: (S)-(-)-4-Isopropyl-2-oxazolidinone, 98% | 17016-83-0
Brand: J&K Chemical
SKU: JK517085_5_G
Price: 142.5 USD
Availability: InStock

Cat. No JK517085_5_G

Vendor: J&K Chemical

Product Information

Product Name

(S)-(-)-4-Isopropyl-2-oxazolidinone, 98%

Brand Name

J&K

Product Number

517085

CAS

17016-83-0

Molecular Formula

C6H11NO2

Molecular Weight

129.16

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

7157133

IUPAC Name

(4S)-4-propan-2-yl-1,3-oxazolidin-2-one

InChI Key

YBUPWRYTXGAWJX-RXMQYKEDSA-N

SMILES

CC(C)C@H1COC(=O)N1

Properties

Melting Point

70-73

Optical Activity

-20° to -16° (C=1, Ethanol)

Safety Information

Precautionary Statement

P262

References Data Source From Pubchem

Atrasentan hydrochloride

Publication Name: Pharmaceutical Substances

Publication Date: 2026

Scaffold modification and synthesis routes for targeting mutant IDH 1: a review

Publication Name: Discover Applied Sciences

Publication Date: 2025-07-01

DOI: 10.1007/s42452-025-07293-7

Synthesis and Biochemical Evaluation of Monocarboxylic GRB2 SH2 Domain Inhibitors

Publication Name: Methods in molecular biology (Clifton, N.J.)

Publication Date: 2023

DOI: 10.1007/978-1-0716-3393-9_15

Taming Nitrene Reactivity with Silver Catalysts

Publication Name: Synlett

Publication Date: 2020-07-29

DOI: 10.1055/s-0040-1707197

SYNTHESIS–SYNLETT Lecture: Toward the Asymmetric Synthesis of Tetrapetalone A: Preparation of an Enantioenriched Indane Intermediate and Strategy for Endgame Glycosylation

Publication Name: Synthesis

Publication Date: 2018-01-05

DOI: 10.1055/s-0036-1591747

(S)-(-)-4-Isopropyl-2-oxazolidinone, 98%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Atrasentan hydrochloride

Scaffold modification and synthesis routes for targeting mutant IDH 1: a review

Synthesis and Biochemical Evaluation of Monocarboxylic GRB2 SH2 Domain Inhibitors

Taming Nitrene Reactivity with Silver Catalysts

SYNTHESIS–SYNLETT Lecture: Toward the Asymmetric Synthesis of Tetrapetalone A: Preparation of an Enantioenriched Indane Intermediate and Strategy for Endgame Glycosylation