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Merck
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524220

Sigma-Aldrich

2,5-二乙氧基苯胺

97%

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About This Item

线性分子式:
(C2H5O)2C6H3NH2
CAS号:
94-85-9
分子量:
181.23
EC 号:
202-369-5
MDL编号:
MFCD00015144
UNSPSC代码:
12352100
PubChem化学物质编号:
24874398
NACRES:
NA.22

方案

97%

表单

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.[1] Phthalimidomethyl derivatives formed by the condensation of 2,5-Diethoxyaniline and phthalimidomethyl could be used for the characterization of amines.[2]

应用

2,5-Diethoxyaniline may be used to synthesize 4-chloro-2′,5′-diethoxy-2-nitrodiphenylamine[3] and methyl 2-chloro-3-(2,5-diethoxyphenyl)propionate.[4]

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H315,H319,H335

危险分类

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 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
08321CO

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Antiulcer activity of 5-benzylthiazolidine-2, 4-dione derivatives.
Sohda T, et al.
Chemical & Pharmaceutical Bulletin, 31(2, 560-569 (1983)
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)
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)
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)

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