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4-氯磺酰基苯甲酸

4-氯磺酰基苯甲酸名称

[ CAS 号 ]:
10130-89-9

[ 中文名 ]:
4-(氯磺酰)苯甲酸

[ 英文名 ]:
4-(Chlorosulfonyl)benzoic acid

[中文别名 ]:

4-(氯磺酰(基))苯甲酸

[英文别名 ]:

4-chlorosulfonylbenzoic acid
MFCD00007448
Benzoic acid, 4-(chlorosulfonyl)-
EINECS 233-367-2
4-(Chlorosulfonyl)benzoic acid

4-氯磺酰基苯甲酸物理化学性质

[ 密度 ]:
1.6±0.1 g/cm3

[ 沸点 ]:
379.1±25.0 °C at 760 mmHg

[ 熔点 ]:
230 °C

[ 分子式 ]:
C₇H₅ClO₄S

[ 分子量 ]:
220.630

[ 闪点 ]:
183.1±23.2 °C

[ 精确质量 ]:
219.959702

[ PSA ]:
79.82000

[ LogP ]:
2.12

[ 外观性状 ]:
灰白色至米色粉末

[ 蒸汽压 ]:
0.0±0.9 mmHg at 25°C

[ 折射率 ]:
1.588

[ 储存条件 ]:
室温

4-氯磺酰基苯甲酸MSDS

4-氯磺酰基苯甲酸安全信息

[ 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) ]:
R22;R29;R34

[ 安全声明 (欧洲) ]:
S8-S45-S36/37/39-S26

[ 危险品运输编码 ]:
3261

[ 包装等级 ]:
II

[ 危险类别 ]:
8

[ 海关编码 ]:
2916399090

4-氯磺酰基苯甲酸合成路线

4-氯磺酰基苯甲酸上下游产品

4-氯磺酰基苯甲酸上游产品

4-氯磺酰基苯甲酸下游产品

4-氯磺酰基苯甲酸海关

[ 海关编码 ]: 2916399090

[ 中文概述 ]:
2916399090 其他芳香一元羧酸. 增值税率:17.0% 退税率:9.0% 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, 丙烯酸、丙烯酸盐或酯应报明包装

[ Summary ]:
2916399090 other aromatic monocarboxylic acids, their anhydrides, halides, peroxides, peroxyacids and their derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

4-氯磺酰基苯甲酸文献

ATP-phosphopeptide conjugates as inhibitors of Src tyrosine kinases.

Bioorg. Med. Chem. 12(22) , 5753-66, (2004)

A number of Src SH2 domain inhibitors enhance the kinase catalytic activity by switching the closed inactive to the open active conformation. ATP-phosphopeptide conjugates were designed and synthesize...

Synthesis and evaluation of a chiral heterogeneous transfer hydrogenation catalyst. Bayston DJ, et al.

Tetrahedron Asymmetry 9(12) , 2015-18, (1998)

Mono-6-(O-2, 4, 6-triisopropylbenzenesulfonyl)-?-cyclodextrin, a novel intermediate for the synthesis of mono-functionalised ?-cyclodextrins. Palin R, et al.

Tetrahedron Lett. 42(50) , 8897-8899, (2001)

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