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1-溴全氟己烷

1-溴全氟己烷名称

[ CAS 号 ]:
335-56-8

[ 中文名 ]:
1-溴全氟乙烷

[ 英文名 ]:
1-bromoperfluorohexane

[中文别名 ]:

[英文别名 ]:

Tridecafluorohexyl Bromide
n-1-bromoperfluorohexane
EINECS 206-391-6
MFCD00042349
1-Bromoperfluorohexane
1-Bromotridecafluorohexane
Perfluorohexyl bromide
bromotridecafluorohexane

1-溴全氟己烷物理化学性质

[ 密度 ]:
1.871 g/mL at 25 °C(lit.)

[ 沸点 ]:
97 °C(lit.)

[ 熔点 ]:
-49ºC

[ 分子式 ]:
C₆BrF₁₃

[ 分子量 ]:
398.94700

[ 闪点 ]:
100-101°C

[ 精确质量 ]:
397.89800

[ LogP ]:
5.07760

[ 外观性状 ]:
无色液体

[ 折射率 ]:
n20/D 1.3(lit.)

[ 储存条件 ]:
室温，干燥

1-溴全氟己烷MSDS

详细MSDS(安全技术说明书)

1-溴全氟己烷安全信息

[ 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 ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ 危害码 (欧洲) ]:
Xi: Irritant;

[ 风险声明 (欧洲) ]:
R36/37/38

[ 安全声明 (欧洲) ]:
S26-S36

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

[ WGK德国 ]:
3

[ 海关编码 ]:
2903799090

1-溴全氟己烷上下游产品

1-溴全氟己烷上游产品

1-溴全氟己烷下游产品

1-溴全氟己烷海关

[ 海关编码 ]: 2903799090

[ 中文概述 ]:
2903799090 其他无环烃卤化衍生物（含二种或三种以上不同卤素）。监管条件:无。增值税率:17.0%。退税率:9.0%。最惠国关税:5.5%。普通关税:30.0%

[ Summary ]:
2903799090 halogenated derivatives of acyclic hydrocarbons containing two or more different halogens。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%

1-溴全氟己烷文献

In vitro cellular effects of perfluorochemicals correlate with their lipid solubility.

Am. J. Physiol. Lung Cell. Mol. Physiol. 278(5) , L1018-24, (2000)

Preclinical studies comparing perflubron partial liquid ventilation with conventional mechanical ventilation have indicated that perflubron partial liquid ventilation may exert some anti-inflammatory ...

A general synthesis of fluoroalkylated alkenes by palladium-catalyzed Heck-type reaction of fluoroalkyl bromides.

Angew. Chem. Int. Ed. Engl. 54(4) , 1270-4, (2015)

An efficient palladium-catalyzed Heck-type reaction of fluoroalkyl halides, including perfluoroalkyl bromides, trifluoromethyl iodides, and difluoroalkyl bromides, has been developed. The reaction pro...

Triphenylsilyl as a protecting group in the synthesis of 1, 12-heterodisubstituted p-carboranes

J. Org. Chem. 65(5) , 1434-41, (2000)

A triphenylsilyl group is used as an auxiliary in the synthesis of heterodisubstituted p-carboranes via triphenylsilyl-p-carborane (1). The preparation of 1 is statistical, but with recovery of the st...

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