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氯代二硫代甲酸五氟苯基酯

氯代二硫代甲酸五氟苯基酯名称

[ CAS 号 ]:
135192-53-9

[ 中文名 ]:
氯代二硫代甲酸五氟苯基酯

[ 英文名 ]:
PENTAFLUOROPHENYL CHLOROTHIONOFORMATE

[中文别名 ]:

[英文别名 ]:

Pentafluorophenyl Chlorothionoformate
Pentafluorophenyl Thionochloroformate
Chlorothioformic Acid O-Pentafluorophenyl Ester
pentafluorophenoxythiocarbonyl chloride
pentafluorophenyloxythiocarbonyl chloride
O-Perfluorophenyl Chlorothioformate
O-pentafluorophenyl chlorothionoformate
O-pentafluorophenyl chlorothioformate
P1267
MFCD00075405

氯代二硫代甲酸五氟苯基酯物理化学性质

[ 密度 ]:
1.635 g/mL at 25ºC(lit.)

[ 沸点 ]:
98-102ºC50 mm Hg(lit.)

[ 分子式 ]:
C₇ClF₅OS

[ 分子量 ]:
262.58400

[ 闪点 ]:
189 °F

[ 精确质量 ]:
261.92800

[ PSA ]:
41.32000

[ LogP ]:
3.28460

[ 外观性状 ]:
固体

[ 蒸汽压 ]:
1.03mmHg at 25°C

[ 折射率 ]:
n20/D 1.481(lit.)

[ 储存条件 ]:
存放于惰性气体之中;避免湿气 (分解)

氯代二硫代甲酸五氟苯基酯MSDS

氯代二硫代甲酸五氟苯基酯安全信息

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

[ 危害码 (欧洲) ]:
C

[ 风险声明 (欧洲) ]:
34

[ 安全声明 (欧洲) ]:
26-27-36/37/39-45

[ 危险品运输编码 ]:
UN 3265 8/PG 2

[ 海关编码 ]:
2930909090

氯代二硫代甲酸五氟苯基酯合成路线

氯代二硫代甲酸五氟苯基酯上下游产品

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氯代二硫代甲酸五氟苯基酯下游产品

氯代二硫代甲酸五氟苯基酯海关

[ 海关编码 ]: 2930909090

[ 中文概述 ]:
2930909090. 其他有机硫化合物. 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:30.0%

[ 申报要素 ]: 品名, 成分含量, 用途

[ Summary ]:
2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

氯代二硫代甲酸五氟苯基酯文献

Regioselective synthesis of beta-N1- and beta-N3-alloxazine nucleosides

Org. Lett. 2(2) , 227-30, (2000)

[structures: see text] A regio- and stereoselective glycosylation of ribose tetraester with persilylated alloxazine to give either beta-N1 or beta-N3 nucleosides is described. The N3 product is potent...

Tuning the acceptors in catalyzed cyclizations initiated by allenes. Silylstannylation/cyclization of allene-aldehydes for synthesis of polyalkylated indolizidines including 223A congeners.

J. Org. Chem. 69(26) , 9151-8, (2004)

Starting from succinamide and 1,2-heptadiene-4-ol, a racemic allene-aldehyde substrate, 20, suitable for R(3)SiSnR'(3)-mediated cyclization was synthesized in six steps and in 21% yield. Stereoselecti...

The invention of radical reactions. Part XXI. Simple methods for the radical deoxygenation of primary alcohols. Barton DHR, et al.

Tetrahedron 47(43) , 8969-94, (1991)

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