4-叠氮苯异硫氰酸酯

4-叠氮苯异硫氰酸酯名称

[ CAS 号 ]:
74261-65-7

[ 中文名 ]:
4-叠氮苯异硫氰酸酯

[ 英文名 ]:
4-azidophenyl isothiocyanate

[中文别名 ]:

4-叠氮基异硫氰酸苯酯

[英文别名 ]:

4-azidophenyl isothiocyante
MFCD00042980
N3PhNCS
4-isothiocyanatophenylazide
4-Azidophenyl isothiocyanate
4-isothiocyanate-phenylazide
para-Azidophenyl isothiocyanate
p-azidophenyl isothiocyanate

4-叠氮苯异硫氰酸酯物理化学性质

[ 熔点 ]:
65-68ºC(lit.)

[ 分子式 ]:
C₇H₄N₄S

[ 分子量 ]:
176.19800

[ 精确质量 ]:
176.01600

[ PSA ]:
94.20000

[ LogP ]:
2.81546

[ 储存条件 ]:
2-8°C

4-叠氮苯异硫氰酸酯MSDS

详细MSDS(安全技术说明书)

4-叠氮苯异硫氰酸酯安全信息

[ 符号 ]:

GHS02, GHS07, GHS08

[ 信号词 ]:
Danger

[ 危害声明 ]:
H228-H302 + H312 + H332-H315-H317-H319-H334-H335

[ 警示性声明 ]:
P210-P261-P280-P305 + P351 + P338-P342 + P311

[ 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) ]:
F: Flammable;Xn: Harmful;

[ 风险声明 (欧洲) ]:
11-20/21/22-36/37/38-42

[ 安全声明 (欧洲) ]:
22-26-36/37/39

[ 危险品运输编码 ]:
UN 1325 4.1/PG 2

[ WGK德国 ]:
3

[ 包装等级 ]:
III

[ 危险类别 ]:
4.1

[ 海关编码 ]:
2930909090

4-叠氮苯异硫氰酸酯海关

[ 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%

4-叠氮苯异硫氰酸酯文献

5-Isothiocyanato-1-naphthalene azide and rho-azidophenylisothiocyanate. Synthesis and application in hydrophobic heterobifunctional photoactive cross-linking of membrane proteins.

Eur. J. Biochem. 125 , 197, (1982)

Two hydrophobic, heterobifunctional azidoarylisothiocyanates have been synthesized. The reagents are applicable for group-directed modification of membrane-integrated protein segments and subsequent p...

Synthesis of transferrin (Tf) conjugated liposomes via Staudinger ligation.

Int. J. Pharm. 404(1-2) , 205-10, (2011)

Staudinger ligation was evaluated as a strategy for synthesizing receptor targeted liposomes. First, an activated lipid derivative was synthesized by reacting dioleoyl phosphatidylethanolamine (DOPE) ...

H. Sigrist, P. Zahler

FEBS Lett. 113 , 307, (1980)

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