(R)-(+)-2-[2-(Diphenylphosphino)phenyl]-4-isopropyl-2-oxazoline, 98%

Name: (R)-(+)-2-[2-(Diphenylphosphino)phenyl]-4-isopropyl-2-oxazoline, 98% | 164858-78-0
Brand: J&K Chemical
SKU: JK547197_250_MG
Price: 90.5 USD
Availability: InStock

Cat. No JK547197_250_MG

Vendor: J&K Chemical

Product Information

Product Name

(R)-(+)-2-2-(Diphenylphosphino)phenyl-4-isopropyl-2-oxazoline, 98%

Brand Name

J&K

Product Number

547197

CAS

164858-78-0

Molecular Formula

C24H24NOP

Molecular Weight

373.43

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

(4R)-2-2-(Diphenylphosphino)phenyl-4,5-dihydro-4-(1-methylethyl)oxazole
(R)-(+)-2-2-(Diphenylphosphino)phenyl-4,5-dihydro-4-isopropyl-oxazole

PubChem CID

2734144

IUPAC Name

diphenyl-2-(4R)-4-propan-2-yl-4,5-dihydro-1,3-oxazol-2-ylphenylphosphane

InChI Key

OUQSAXROROGQEE-QFIPXVFZSA-N

SMILES

CC(C)C@@H1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C4=CC=CC=C4

Properties

Melting Point

85-90

Optical Activity

+45° to +51° (C = 1.4% in chloroform)

References Data Source From Pubchem

Short and Straightforward Enantioselective Synthesis of Both Enantiomers of Mequitazine through Iridium-Catalyzed Asymmetric Hydrogenation of a Nonfunctionalized Cyclic Enamine

Publication Name: Synlett

Publication Date: 2014-05-14

DOI: 10.1055/s-0033-1341274

Detour and Direct Induction of Methyl-Containing Chiral Centers via Catalytic C–H or C–C Bond Formation

Publication Name: Synthesis

Publication Date: 2012-04-17

DOI: 10.1055/s-0031-1290869

Reactions of 2,3-Dihydrofuran and 2,2-Dialkyl-2,3-dihydrofurans

Publication Name: Science of Synthesis

Publication Date: 2012

Preparation of Dialkyl Sulfides

Publication Name: Science of Synthesis

Publication Date: 2011

Synthesis of P-Stereogenic Phosphines

Publication Name: Synfacts

Publication Date: 2006-06

DOI: 10.1055/s-2006-941821