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2,4-二氯-5-硝基三氟甲基苯

2,4-二氯-5-硝基三氟甲基苯名称

[ CAS 号 ]:
400-70-4

[ 中文名 ]:
2,4-二氯-5-硝基三氟甲基苯

[ 英文名 ]:
2,4-Dichloro-5-nitrobenzotrifluoride

[中文别名 ]:

[英文别名 ]:

Benzene, 1,5-dichloro-2-nitro-4-(trifluoromethyl)-
MFCD00007073
2,4-Dichloro-5-Nitro benzotrifluoride
2,4-Dichloro-5-Nitrobenzotrifluoride
1,5-Dichloro-2-nitro-4-(trifluoromethyl)benzene

2,4-二氯-5-硝基三氟甲基苯物理化学性质

[ 密度 ]:
1.6±0.1 g/cm3

[ 沸点 ]:
264.9±35.0 °C at 760 mmHg

[ 熔点 ]:
55-57 °C(lit.)

[ 分子式 ]:
C₇H₂Cl₂F₃NO₂

[ 分子量 ]:
259.997

[ 闪点 ]:
114.0±25.9 °C

[ 精确质量 ]:
258.941467

[ PSA ]:
45.82000

[ LogP ]:
3.88

[ 外观性状 ]:
黄色晶体

[ 蒸汽压 ]:
0.0±0.5 mmHg at 25°C

[ 折射率 ]:
1.511

[ 储存条件 ]:
室温

2,4-二氯-5-硝基三氟甲基苯MSDS

2,4-二氯-5-硝基三氟甲基苯安全信息

[ 符号 ]:

GHS07

[ 信号词 ]:
Warning

[ 危害声明 ]:
H315-H319-H335

[ 警示性声明 ]:
P261-P305 + P351 + P338

[ 个人防护装备 ]:
dust mask type N95 (US);Eyeshields;Gloves

[ 危害码 (欧洲) ]:
Xn:Harmful;

[ 风险声明 (欧洲) ]:
R20/21/22;R36/37/38

[ 安全声明 (欧洲) ]:
S26-S37/39-S36/37/39

[ 危险品运输编码 ]:
NONH for all modes of transport

[ WGK德国 ]:
3

[ 海关编码 ]:
2904909090

2,4-二氯-5-硝基三氟甲基苯合成路线

2,4-二氯-5-硝基三氟甲基苯上下游产品

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2,4-二氯-5-硝基三氟甲基苯下游产品

2,4-二氯-5-硝基三氟甲基苯海关

[ 海关编码 ]: 2904909090

[ 中文概述 ]:
2904909090 其他烃的磺化、硝化、亚硝化衍生物（不论是否卤化）. 增值税率:17.0% 退税率:9.0% 监管条件:无最惠国关税:5.5% 普通关税:30.0%

[ 申报要素 ]: 品名, 成分含量, 用途

[ Summary ]:
HS:2904909090 sulphonated, nitrated or nitrosated derivatives of hydrocarbons, whether or not halogenated VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

2,4-二氯-5-硝基三氟甲基苯文献

Quantitative structure-activity relationships: analysis of interactions of 2,3,7,8-tetrachlorodibenzo-p-dioxin and 2-substituted analogues with rat, mouse, guinea pig, and hamster cytosolic receptor.

Cancer Res. 47(19) , 5108-5111, (1987)

The competitive receptor binding affinities of thirteen 2-substituted 3,7,8-trichlorodibenzo-p-dioxins to hepatic cytosol from rat, mouse, guinea pig, and hamster were determined with [3H]-2,3,7,8-tet...

Synthesis, spectral characterization, and biological activity of some new substituted 10H-phenothiazines, its ribofuranosides, and sulfones.

Nucleosides Nucleotides Nucleic Acids 29(3) , 178-89, (2010)

This article describes the synthesis of new substituted 10 H-phenothiazines by Smiles rearrangement. These compounds are then used as a base to form ribofuranosides by treating them with a sugar (1-O-...

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