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氯代二硫代甲酸苯酯

氯代二硫代甲酸苯酯名称

[ CAS 号 ]:
16911-89-0

[ 中文名 ]:
氯代二硫代甲酸苯基酯

[ 英文名 ]:
PHENYL CARBONOCHLORIDODITHIOATE

[中文别名 ]:

氯代二硫代甲酸苯酯

[英文别名 ]:

Phenyldithiokohlensaeure-chlorid
phenyl chlorodithioformate
phenyl chloridodithiocarbonate
Chlorodithiokohlensaeure-phenylester
chlorodithioformic acid phenyl ester
Phenyl carbonochloridodithioate
Dithiokohlensaeure-S-phenylester-chlorid
MFCD00013429
Carbonochloridodithioic acid,phenyl ester
dithiocarbonochloridic acid phenyl ester

氯代二硫代甲酸苯酯物理化学性质

[ 密度 ]:
1.331 g/mL at 25ºC(lit.)

[ 沸点 ]:
135ºC15 mm Hg(lit.)

[ 分子式 ]:
C₇H₅ClS₂

[ 分子量 ]:
188.69800

[ 闪点 ]:
>230 °F

[ 精确质量 ]:
187.95200

[ PSA ]:
57.39000

[ LogP ]:
3.30240

[ 外观性状 ]:
液体;Light yellow to Amber to Dark green clear liquid

[ 蒸汽压 ]:
0.00964mmHg at 25°C

[ 折射率 ]:
n20/D 1.6688(lit.)

[ 储存条件 ]:
0-10°C;存放于惰性气体之中;避免湿气 (分解)

氯代二硫代甲酸苯酯MSDS

详细MSDS(安全技术说明书)

氯代二硫代甲酸苯酯安全信息

[ 符号 ]:

GHS05, GHS07

[ 信号词 ]:
Danger

[ 危害声明 ]:
H302-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: Corrosive;

[ 风险声明 (欧洲) ]:
22-34

[ 安全声明 (欧洲) ]:
26-36/37/39-45

[ 危险品运输编码 ]:
UN 1760 8/PG 3

[ 包装等级 ]:
III

[ 海关编码 ]:
2930909090

氯代二硫代甲酸苯酯合成路线

详细合成路线

氯代二硫代甲酸苯酯上下游产品

氯代二硫代甲酸苯酯上游产品

氯代二硫代甲酸苯酯下游产品

氯代二硫代甲酸苯酯海关

[ 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%

氯代二硫代甲酸苯酯文献

Kinetics and mechanism of the reactions of aryl chlorodithioformates with pyridines and secondary alicyclic amines. Castro EA, et al.

J. Phys. Org. Chem. 22(11) , 1030-37, (2009)

Synthesis of Phenyl Arylsulfonyl-alkyl-dithiocarbamates and Their Hydrolytic Reactivity in Hydroxide and Hydroperoxide Media. Norberto F, et al.

European J. Org. Chem. 2005(21) , 4710-14, (2005)

The nucleofuge in the pyridinolysis of O-(4-nitrophenyl) S-aryl thio and dithiocarbonates. Castro EA, et al.

J. Phys. Org. Chem. 25(11) , 994, (2012)

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