推薦產品
化驗
99%
形狀
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.)
官能基
ether
phenyl
SMILES 字串
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 密鑰
ZXTHWIZHGLNEPG-UHFFFAOYSA-N
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
235.4 °F - closed cup
閃點（°C）
113 °C - closed cup
個人防護裝備
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
從最近期的版本中選擇一個：
分析證明 (COA)
Lot/Batch Number
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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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