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3,5-双(三氟甲基)苯-1-磺酰氯

3,5-双(三氟甲基)苯-1-磺酰氯名称

[ CAS 号 ]:
39234-86-1

[ 中文名 ]:
3,5-二三氟甲基苯磺酰氯

[ 英文名 ]:
3,5-Bis(trifluoromethyl)benzene-1-sulfonyl chloride

[中文别名 ]:

[英文别名 ]:

3,5-bis(trifluoromethyl)benzene sulfonyl chloride
EINECS 254-371-0
MFCD00014725
WSGR CXFFF EXFFF
3,5-(bistrifluoromethyl)phenylsulfonyl chloride
3,5-Bis(trifluoromethyl)benzenesulphonyl chloride
3,5-di(trifluoromethyl)benzenesulfonyl chloride
3,5-Di(trifluoromethyl)benzene-1-sulfonyl chloride
3,5-Bis(trifluoromethyl)benzenesulfonyl chloride

3,5-双(三氟甲基)苯-1-磺酰氯物理化学性质

[ 密度 ]:
1.6±0.1 g/cm3

[ 沸点 ]:
248.3±40.0 °C at 760 mmHg

[ 熔点 ]:
34-38 °C(lit.)

[ 分子式 ]:
C₈H₃ClF₆O₂S

[ 分子量 ]:
312.617

[ 闪点 ]:
104.0±27.3 °C

[ 精确质量 ]:
311.944641

[ PSA ]:
42.52000

[ LogP ]:
4.07

[ 蒸汽压 ]:
0.0±0.5 mmHg at 25°C

[ 折射率 ]:
1.435

[ 储存条件 ]:
Refrigerator

3,5-双(三氟甲基)苯-1-磺酰氯MSDS

3,5-双(三氟甲基)苯-1-磺酰氯安全信息

[ 符号 ]:

GHS05

[ 信号词 ]:
Danger

[ 危害声明 ]:
H314

[ 警示性声明 ]:
P280-P305 + P351 + P338-P310

[ 个人防护装备 ]:
Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges

[ 危害码 (欧洲) ]:
C:Corrosive;

[ 风险声明 (欧洲) ]:
R34

[ 安全声明 (欧洲) ]:
S26-S36-S36/37/39

[ 危险品运输编码 ]:
UN 3261 8/PG 2

[ WGK德国 ]:
3

[ 包装等级 ]:
III

[ 危险类别 ]:
8

[ 海关编码 ]:
2904909090

3,5-双(三氟甲基)苯-1-磺酰氯合成路线

3,5-双(三氟甲基)苯-1-磺酰氯上下游产品

3,5-双(三氟甲基)苯-1-磺酰氯上游产品

3,5-双(三氟甲基)苯-1-磺酰氯下游产品

3,5-双(三氟甲基)苯-1-磺酰氯海关

[ 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%

3,5-双(三氟甲基)苯-1-磺酰氯文献

New library of aminosulfonyl-tagged Hoveyda-Grubbs type complexes: Synthesis, kinetic studies and activity in olefin metathesis transformations.

Beilstein J. Org. Chem. 6 , 1159-66, (2010)

Seven novel Hoveyda-Grubbs precatalysts bearing an aminosulfonyl function are reported. Kinetic studies indicate an activity enhancement compared to Hoveyda's precatalyst. A selection of these catalys...

Highly enantioselective catalytic thiolysis of prochiral cyclic dicarboxylic anhydrides utilizing a bifunctional chiral sulfonamide.

Angew. Chem. Int. Ed. Engl. 44(36) , 5838-41, (2005)

Versatile chiral reagent for the highly enantioselective synthesis of either anti or syn ester aldols. Corey EJ and Kim SS.

J. Am. Chem. Soc. 112(12) , 4976-4977, (1990)

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