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3-三氟甲基吡唑

3-三氟甲基吡唑名称

[ CAS 号 ]:
20154-03-4

[ 中文名 ]:
3-(三氟甲基)吡唑

[ 英文名 ]:
3-(Trifluoromethyl)pyrazole

[中文别名 ]:

[英文别名 ]:

AKOS PAO-1199
3-(Trifluoromethyl)pyrazole
BUTTPARK 29 8-71
MFCD00115018
TRIFLUOROMETHYLPYRAZOLE
3-CF3-pyrazole
1H-Pyrazole, 3-(trifluoromethyl)-
3-(Trifluoromethyl)-1H-pyrazole
3-trifluromethyl-pyrazol
1H-3-trifluoromethylpyrazol

3-三氟甲基吡唑物理化学性质

[ 密度 ]:
1.4±0.1 g/cm3

[ 沸点 ]:
177.7±35.0 °C at 760 mmHg

[ 熔点 ]:
45-47 °C(lit.)

[ 分子式 ]:
C₄H₃F₃N₂

[ 分子量 ]:
136.075

[ 闪点 ]:
61.3±25.9 °C

[ 精确质量 ]:
136.024826

[ PSA ]:
28.68000

[ LogP ]:
1.29

[ 外观性状 ]:
无色至淡黄色液体

[ 蒸汽压 ]:
1.4±0.3 mmHg at 25°C

[ 折射率 ]:
1.417

[ 储存条件 ]:
室温，避光，干燥

3-三氟甲基吡唑MSDS

3-三氟甲基吡唑安全信息

[ 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) ]:
Xi:Irritant;

[ 风险声明 (欧洲) ]:
R36/37/38

[ 安全声明 (欧洲) ]:
S26-S36-S37/39

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

[ WGK德国 ]:
3

[ 海关编码 ]:
2942000000

3-三氟甲基吡唑合成路线

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3-三氟甲基吡唑海关

[ 海关编码 ]: 2933199090

[ 中文概述 ]:
2933199090. 其他结构上有非稠合吡唑环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%

[ 申报要素 ]: 品名, 成分含量, 用途, 乌洛托品请注明外观, 6－己内酰胺请注明外观, 签约日期

[ Summary ]:
2933199090. other compounds containing an unfused pyrazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

3-三氟甲基吡唑文献

Neuronal and non-neuronal bradykinin receptors are involved in the contraction and/or relaxation to the pig bladder neck smooth muscle.

Neurourol. Urodyn. 33(5) , 558-65, (2014)

The current study investigates the role played by bradykinin (BK) receptors in the contractility to the pig bladder neck smooth muscle.Bladder neck strips were mounted in myographs for isometric force...

Insecticidal anthranilic diamides: a new class of potent ryanodine receptor activators.

Bioorg. Med. Chem. Lett. 15 , 4898-906, (2005)

A novel class of anthranilic diamides has been discovered with exceptional insecticidal activity on a range of Lepidoptera. These compounds have been found to exhibit their action by release of intrac...

Fluorous synthesis of disubstituted pyrimidines.

Org. Lett. 5(7) , 1011-3, (2003)

[reaction: see text] The fluorous synthesis of disubstituted pyrimidines is carried out by attaching 2,4-dichloro-6-methylpyrimidine with 1H,1H,2H,2H-perfluorodecanethiol. The tagged substrate is subs...

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