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Merck
CN

527696

Sigma-Aldrich

2,4-二硝基苯甲腈

97%

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线性分子式:
(O2N)2C6H3CN
CAS号:
分子量:
194.12
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

检测方案

97%

mp

100-103 °C (lit.)

SMILES字符串

[O-][N+](=O)c1ccc(C#N)c(c1)[N+]([O-])=O

InChI

1S/C7H3N3O4/c8-4-5-1-2-6(9(11)12)3-7(5)10(13)14/h1-3H

InChI key

KCUDEOWPXBMDJE-UHFFFAOYSA-N

一般描述

2,4-Dinitrobenzonitrile is formed as one of the reaction products from the elimination reactions of (E)-2,4-dinitrobenzaldehyde O-aryloximes. (E)-2,4-Dinitrobenzonitrile is obtained from the reaction between (E)-2,4-dinitrobenzaldehyde O-benzoyloxime with i-Pr2NH in methylcyanide.

应用

2,4-Dinitrobenzonitrile may be used to synthesize N′-hydroxy-2,4-dinitrobenzimidamide.

象形图

FlameExclamation mark

警示用语:

Danger

危险分类

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Flam. Sol. 1

WGK

WGK 3

闪点(°F)

55.0 °F

闪点(°C)

12.78 °C

个人防护装备

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

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Elimination reactions of (E)-2, 4-dinitrobenzaldehyde O-aryloximes promoted by RO-/ROH buffers in EtOH.
Cho BR, et al.
The Journal of Organic Chemistry, 63(9), 3006-3009 (1998)
Elimination Reactions of (E)-2, 4-Dinitrobenzaldehyde O-Benzoyloximes.
Cho BR, et al.
The Journal of Organic Chemistry, 64(22), 8375-8378 (1999)
Synthesis and Properties of Energetic 1, 2, 4-Oxadiazoles.
Wang Z, et al.
European Journal of Organic Chemistry, 34, 7468-7474 (2015)

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