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369756

Sigma-Aldrich

2-Phenyl-2-oxazoline

99%

Synonym(s):

2-Phenyl-1,3-oxazoline, 2-Phenyl-4,5-dihydro-1,3-oxazole, 2-Phenyl-4,5-dihydrooxazole, 4,5-Dihydro-2-phenyloxazole

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About This Item

Empirical Formula (Hill Notation):
C9H9NO
CAS Number:
Molecular Weight:
147.17
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

form

liquid

refractive index

n20/D 1.567 (lit.)

bp

75 °C/0.3 mmHg (lit.)

mp

12 °C (lit.)

density

1.118 g/mL at 25 °C (lit.)

SMILES string

C1CN=C(O1)c2ccccc2

InChI

1S/C9H9NO/c1-2-4-8(5-3-1)9-10-6-7-11-9/h1-5H,6-7H2

InChI key

ZXTHWIZHGLNEPG-UHFFFAOYSA-N

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Ignacio Del Río et al.
Acta crystallographica. Section E, Structure reports online, 65(Pt 1), m103-m104 (2008-01-01)
The title material, [Zn(C(5)H(7)O(2))(2)(C(9)H(9)NO)], was synthesized by the treatment of bis-(acetyl-acetonato)zinc(II) monohydrate with 2-phenyl-2-oxazoline. The Zn atom is coordinated by two chelating acetyl-acetonate groups and one oxazoline ligand in the apical position of a slightly distorted square-pyramidal metal-ligand geometry.
Robert A Gossage et al.
Dalton transactions (Cambridge, England : 2003), (23)(23), 3115-3122 (2008-06-04)
The treatment of cold ( approximately 3 degrees C) methanolic solutions of Li(2)PdCl(4) with two equivalents of 2-phenyl-2-oxazoline (Phox) results in the isolation of [PdCl(2)(Phox)(2)] (3). This complex undergoes remarkably slow isomerisation (CHCl(3)-d) at room temperature to a corresponding thermodynamic
One-pot synthesis of 2-phenyl-2-oxazoline-containing quasi-diblock copoly (2-oxazoline) s under microwave irradiation.
Hoogenboom R, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 45(3), 416-422 (2007)
Microwave Accelerated Polymerization of 2-Phenyl-2-oxazoline.
Sinnwell S and Ritter H.
Macromolecular Rapid Communications, 26(3), 160-163 (2005)
Indira Fabre et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(23), 7595-7604 (2013-04-19)
The activation of the C-H bond of 1-phenylpyrazole (2) and 2-phenyl-2-oxazoline (3) by [Ru(OAc)2(p-cymene)] is an autocatalytic process catalyzed by the co-product HOAc. The reactions are indeed faster in the presence of acetic acid and water but slower in the

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