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三苯基膦氯金

三苯基膦氯金用途

三苯基膦氯金是一种生物化学试剂,可作为生物材料或有机化合物进行生命科学相关研究。

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三苯基膦氯金名称

[ CAS 号 ]:
14243-64-2

[ 中文名 ]:
(三苯基膦)氯化金(I)

[ 英文名 ]:
Gold(1+) chloride-triphenylphosphine (1:1:1)

[中文别名 ]:

[英文别名 ]:

Gold(1+) chloride - triphenylphosphine (1:1:1)
(Triphenylphosphine)gold(I) Chloride
EINECS 238-117-6
Chloro(triphenylphosphine)gold
(Ph3P)AuCl (Triphenylphosphinegold(I) chloride
MFCD00009588
chlorogold,triphenylphosphane

三苯基膦氯金生物活性

[ 描述 ]:

三苯基膦氯金是一种生物化学试剂,可作为生物材料或有机化合物进行生命科学相关研究。

[ 相关类别 ]:

研究领域 >> 其他

信号通路 >> 其他 >> 其他

三苯基膦氯金物理化学性质

[ 沸点 ]:
360ºC at 760 mmHg

[ 熔点 ]:
248-249°C

[ 分子式 ]:
C₁₈H₁₅AuClP

[ 分子量 ]:
494.71

[ 闪点 ]:
181.7ºC

[ 精确质量 ]:
494.026489

[ PSA ]:
13.59000

[ LogP ]:
4.13180

[ 外观性状 ]:
白色到黄色粉末或晶体

[ 蒸汽压 ]:
4.74E-05mmHg at 25°C

[ 储存条件 ]:
Store under Nitrogen

三苯基膦氯金MSDS

三苯基膦氯金安全信息

[ 符号 ]:

GHS07

[ 信号词 ]:
Warning

[ 危害声明 ]:
H315-H319-H335

[ 警示性声明 ]:
P261-P305 + P351 + P338

[ 个人防护装备 ]:
dust mask type N95 (US);Eyeshields;Gloves

[ 危害码 (欧洲) ]:
Xi:Irritant;

[ 风险声明 (欧洲) ]:
R36/37/38

[ 安全声明 (欧洲) ]:
S26-S36/37/39-S37/39

[ 危险品运输编码 ]:
NONH for all modes of transport

三苯基膦氯金合成路线

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三苯基膦氯金文献

A mass spectrometric investigation of the binding of gold antiarthritic agents and the metabolite [Au(CN)2]- to human serum albumin.

J. Biol. Inorg. Chem. 11(5) , 559-70, (2006)

Electrospray ionisation (ESI) mass spectrometry was used to examine the reactions of the clinically used antiarthritic agent [Au(S2O3)2]3-, and AuPEt3Cl, a derivative of another clinically used agent ...

Development of a gold-multifaceted catalysis approach to the synthesis of highly substituted pyrroles: mechanistic insights via Huisgen cycloaddition studies.

J. Org. Chem. 78(3) , 920-34, (2013)

A novel gold-catalyzed method for the regioselective synthesis of highly substituted pyrroles directly from oximes and alkynes was developed via independent optimization of two key steps of the proces...

A powerful chiral counterion strategy for asymmetric transition metal catalysis.

Science 317 , 496-499, (2007)

Traditionally, transition metal-catalyzed enantioselective transformations rely on chiral ligands tightly bound to the metal to induce asymmetric product distributions. Here we report high enantiosele...

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