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Sigma-Aldrich

2-Phenyl-2-oxazoline

99%

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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
Empirical Formula (Hill Notation):
C9H9NO
CAS Number:
7127-19-7
Molecular Weight:
147.17
MDL number:
MFCD00075541
PubChem Substance ID:
24863039
NACRES:
NA.22

Quality Level

100

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

Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315 - H319 - H335

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

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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)
Andrew M Kelly et al.
Macromolecular rapid communications, 32(22), 1815-1819 (2011-09-21)
A 32-membered library of poly(2-oxazoline)-based hydrogels of the composition pEtOx(m) -pPhOx(n) -pPBO(q) (m/n = 150/0, 100/50, 50/100, and 0/150; q = 1.5-30) was prepared from 2-ethyl- (EtOx), 2-phenyl-2-oxazoline (PhOx), and phenylene-1,3-bis-(2-oxazoline) (PBO). The polymerizations were performed from ground monomer mixtures
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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