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质量水平
方案
95%
沸点
170 °C/18 mmHg (lit.)
mp
47-49 °C (lit.)
官能团
phenoxy
SMILES字符串
Nc1ccccc1Oc2ccccc2
InChI
1S/C12H11NO/c13-11-8-4-5-9-12(11)14-10-6-2-1-3-7-10/h1-9H,13H2
InChI key
NMFFUUFPJJOWHK-UHFFFAOYSA-N
一般描述
2-Phenoxyaniline forms crystalline 2:1 (host-to-guest) inclusion complexes with β-cyclodextrin.
应用
2-Phenoxyaniline may be used in the preparation of sodium primary amide complex, 2-PhOC6H4NHNa·NMe[(CH2)2NMe2]2. It was used in the preparation of 2-acetoaminodiphenyl ether. It may be used in the preparation of 4-methyl-2-(2-phenoxyphenyl)azo-phenol.
警示用语：
Warning
危险分类
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
235.4 °F - closed cup
闪点(°C)
113 °C - closed cup
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
The first structurally characterised sodium primary amide complex; synthesis and crystal structure of 2-PhOC6H4NHNa? NMe [(CH2) 2NMe2] 2.
Cragg-Hine I, et al.
J. Chem. Soc., Dalton Trans., 19, 2901-2902 (1994)
Ferenc Szurdoki et al.
Journal of agricultural and food chemistry, 50(1), 29-40 (2002-01-05)
Sensitive and selective enzyme-linked immunosorbent assays (ELISAs) in the immobilized antigen format were developed for fenoxycarb (1), an insect growth regulator (IGR). The parent molecule [ethyl 2-(4-phenoxyphenoxy)ethylcarbamate] was derivatized at several positions to obtain haptens (2-5) that were used to
Susana S Braga et al.
Organic & biomolecular chemistry, 1(5), 873-878 (2003-08-22)
Crystalline 1:1 inclusion complexes with beta-cyclodextrin (beta-CD) and the sodium salt of nimesulide (4-nitro-2-phenoxymethanesulfonanilide), and the sodium salt of the derivative 2-phenoxymethanesulfonanilide, have been prepared by co-precipitation from aqueous solution. The presence of true inclusion complexes was supported by elemental
Synthesis and Pharmacological Evaluation of Certain Schiff Bases and Thiazoldine derivatives as AT1 angiotension-II (AII) receptor antagonists.
Shreenivas MT, et al.
Journal of Pharmaceutical Science and Technology, 1(2), 88-94 (2009)
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