Merck
CN

369756

Sigma-Aldrich

2-苯基-2-噁唑啉

99%

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别名:
2-Phenyl-1,3-oxazoline, 2-Phenyl-4,5-dihydro-1,3-oxazole, 2-Phenyl-4,5-dihydrooxazole, 4,5-Dihydro-2-phenyloxazole
经验公式(希尔记法):
C9H9NO
CAS号:
分子量:
147.17
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

99%

形式

liquid

折射率

n20/D 1.567 (lit.)

bp

75 °C/0.3 mmHg (lit.)

mp

12 °C (lit.)

密度

1.118 g/mL at 25 °C (lit.)

SMILES字符串

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

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

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

靶器官

Respiratory system

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

235.4 °F - closed cup

闪点(°C)

113 °C - closed cup

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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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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