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检测方案
97%
形式
solid
mp
85-88 °C (lit.)
SMILES字符串
CCOc1ccc(OCC)c(N)c1
InChI
1S/C10H15NO2/c1-3-12-8-5-6-10(13-4-2)9(11)7-8/h5-7H,3-4,11H2,1-2H3
InChI key
XPKFTIYOZUJAGA-UHFFFAOYSA-N
一般描述
2,5-Diethoxyaniline is a primary aromatic amine. It can be obtained from 2,5-diethoxynitrobenzene, via reduction with Me3SiSNa. Phthalimidomethyl derivatives formed by the condensation of 2,5-Diethoxyaniline and phthalimidomethyl could be used for the characterization of amines.
应用
2,5-Diethoxyaniline may be used to synthesize 4-chloro-2′,5′-diethoxy-2-nitrodiphenylamine and methyl 2-chloro-3-(2,5-diethoxyphenyl)propionate.
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
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Antiulcer activity of 5-benzylthiazolidine-2, 4-dione derivatives.
Sohda T, et al.
Chemical & Pharmaceutical Bulletin, 31(2, 560-569 (1983)
Direct ring closure through the nitro group. Isomer formation in the synthesis of unsymmetrical phenazines, and some general observations on the phenazine syntheses.
Vivian DL ,et al.
The Journal of Organic Chemistry, 16(1), 1-7 (1951)
Reduction of aromatic nitro compounds to aromatic amines by sodium trimethylsilanethiolate.
Hwu JR, et al.
The Journal of Organic Chemistry, 57(19), 5254-5255 (1992)
Identification of Amines. II. Phthalimidomethyl Derivatives of Primary and Secondary Amines1.
Heine HW, et al.
Journal of the American Chemical Society, 78(3), 672-674 (1956)
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