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5-甲基-2-硝基苯胺

5-甲基-2-硝基苯胺用途

用于有机合成中间体

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5-甲基-2-硝基苯胺名称

[ CAS 号 ]:
578-46-1

[ 中文名 ]:
5-甲基-2-硝基苯胺

[ 英文名 ]:
5-Methyl-2-nitroaniline

[中文别名 ]:

[英文别名 ]:

5-Methyl-2-nitroaniline
Benzenamine, 5-methyl-2-nitro-
MFCD00007814
EINECS 209-423-7

5-甲基-2-硝基苯胺物理化学性质

[ 密度 ]:
1.3±0.1 g/cm3

[ 沸点 ]:
312.4±22.0 °C at 760 mmHg

[ 熔点 ]:
110-111 °C(lit.)

[ 分子式 ]:
C₇H₈N₂O₂

[ 分子量 ]:
152.151

[ 闪点 ]:
142.8±22.3 °C

[ 精确质量 ]:
152.058578

[ PSA ]:
71.84000

[ LogP ]:
2.29

[ 外观性状 ]:
橙色粉末

[ 蒸汽压 ]:
0.0±0.7 mmHg at 25°C

[ 折射率 ]:
1.616

[ 储存条件 ]:
室温

5-甲基-2-硝基苯胺MSDS

5-甲基-2-硝基苯胺毒性和生态

CHEMICAL IDENTIFICATION

RTECS NUMBER :: XU8060000

CHEMICAL NAME :: m-Toluidine, 6-nitro-

CAS REGISTRY NUMBER :: 578-46-1

BEILSTEIN REFERENCE NO. :: 2691416

LAST UPDATED :: 199803

DATA ITEMS CITED :: 1

MOLECULAR FORMULA :: C7-H8-N2-O2

MOLECULAR WEIGHT :: 152.17

WISWESSER LINE NOTATION :: WNR BZ D1

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

MUTATION DATA

TYPE OF TEST :: Mutation in microorganisms

TEST SYSTEM :: Bacteria - Salmonella typhimurium

DOSE/DURATION :: 500 ug/plate

REFERENCE :: ENMUDM Environmental Mutagenesis. (New York, NY) V.1-9, 1979-87. For publisher information, see EMMUEG. Volume(issue)/page/year: 4,163,1982

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5-甲基-2-硝基苯胺安全信息

[ 符号 ]:

GHS06, GHS08, GHS09

[ 信号词 ]:
Danger

[ 危害声明 ]:
H301 + H311 + H331-H373-H411

[ 警示性声明 ]:
P261-P273-P280-P301 + P310-P311

[ 危害码 (欧洲) ]:
T: Toxic;N: Dangerous for the environment;

[ 风险声明 (欧洲) ]:
R23/24/25;R33;R51/53

[ 安全声明 (欧洲) ]:
S28-S36/37-S45-S61

[ 危险品运输编码 ]:
UN 2660 6.1/PG 3

[ WGK德国 ]:
3

[ RTECS号 ]:
XU8060000

[ 包装等级 ]:
III

[ 危险类别 ]:
6.1

[ 海关编码 ]:
2921430090

5-甲基-2-硝基苯胺合成路线

5-甲基-2-硝基苯胺上下游产品

5-甲基-2-硝基苯胺上游产品

5-甲基-2-硝基苯胺下游产品

5-甲基-2-硝基苯胺海关

[ 海关编码 ]: 2921430090

[ 中文概述 ]:
2921430090 甲苯胺及其衍生物以及它们的盐. 增值税率:17.0% 退税率:9.0% 监管条件:无最惠国关税:6.5% 普通关税:30.0%

[ 申报要素 ]: 品名, 成分含量, 用途, 原产地证据文件及编号(例附原产地证书, 原产于欧盟的

[ Summary ]:
HS:2921430090 toluidines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

5-甲基-2-硝基苯胺文献

Synthesis and histone deacetylase inhibitory activity of new benzamide derivatives.

J. Med. Chem. 42(15) , 3001-3, (1999)

Newly synthesized benzamide derivatives were evaluated for their inhibitory activity against histone deacetylase. The structure of these derivatives was unrelated to the known inhibitors, and IC(50) v...

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