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29892-37-3

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29892-37-3 Usage

Description

(DIMETHYLSULFIDE)GOLD(I) CHLORIDE, also known as Chloro(dimethylsulfide)gold(I), is a chemical compound that plays a significant role in the synthesis of various gold(I)-catalysts. It is characterized by its ability to facilitate chemical reactions under mild conditions, making it a valuable component in the field of organic chemistry.

Uses

Used in Chemical Synthesis:
(DIMETHYLSULFIDE)GOLD(I) CHLORIDE is used as a catalyst for the intermolecular [2+2] cycloaddition of terminal alkynes with substituted alkenes to form substituted cyclobutenes. This application is particularly useful in the synthesis of complex organic molecules and pharmaceutical compounds.
Used in Catalyst Development:
(DIMETHYLSULFIDE)GOLD(I) CHLORIDE is used as a precursor in the development of various gold(I)-catalysts, including:
1. Chloro(trimesitylphosphine)gold(I) complexes: These complexes are employed in the catalysis of various organic reactions, enhancing the efficiency and selectivity of the processes.
2. Gold(I) N-heterocyclic carbene (NHC) complexes: These complexes are versatile catalysts for a wide range of organic transformations, including C-C and C-H bond formations.
3. Bis(carbene)gold(I) complex of ferrocenyl complexes: These complexes are used in the catalysis of redox reactions and have potential applications in the synthesis of pharmaceuticals and other specialty chemicals.
4. Gold(I) acetylide complexes: These complexes are utilized in the formation of carbon-carbon triple bonds, which are essential in the synthesis of various organic compounds and materials.

Reaction

Gold(I) precursor to more advanced gold catalysts Gold catalyst for the conversion of propargyl sulfoxides to α-thioenones.

Check Digit Verification of cas no

The CAS Registry Mumber 29892-37-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,8,9 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 29892-37:
(7*2)+(6*9)+(5*8)+(4*9)+(3*2)+(2*3)+(1*7)=163
163 % 10 = 3
So 29892-37-3 is a valid CAS Registry Number.

29892-37-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (Dimethylsulfide)gold(I) chloride

1.2 Other means of identification

Product number -
Other names (Dimethylsulfide)gold(I) Chloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:29892-37-3 SDS

29892-37-3Relevant articles and documents

Novel gold(I)- and gold(III)-N-heterocyclic carbene complexes: Synthesis and evaluation of their anticancer properties

Rana, Bidyut Kumar,Nandy, Abhishek,Bertolasi, Valerio,Bielawski, Christopher W.,Das Saha, Krishna,Dinda, Joydev

, p. 2544 - 2548 (2014)

A novel Au(III)-N-heterocyclic carbene organometallic complex supported by two N-heterocyclic carbene (NHC) ligands was synthesized from Au(SMe 2)Cl and 1-methyl-2-pyridin-2-yl-2H-imidazo[1,5-a]pyridin-4-ylium hexafluorophosphate via a Ag intermediate. X-ray crystallography revealed the first example of a square planar geometry adopted by a Au(III) species stabilized by two NHCs and two chloride ligands. The aforementioned Au(I)- and Au(III)-NHC complexes were found to be more potent than cisplatin against the HCT 116, HepG2, A549, and MCF7 cell lines.

Synthesis, Characterization, and in vitro Cytotoxicity of Gold(I) Complexes of 2-(Diphenylphosphanyl)ethylamine and Dithiocarbamates

Sulaiman, Adam A. A.,Altaf, Muhammad,Isab, Anvarhusein A.,Alawad, Abdullah,Altuwaijri, Saleh,Ahmad, Saeed

, p. 1454 - 1459 (2016)

Gold(I) complexes of 2-(diphenylphosphanyl)ethylamine or (2-aminoethyl)diphenylphosphine (AEP), and dithiocaarbamates (R2NCS2) were prepared by the reaction of these ligands with (CH3)2S-AuCl in dichloromethane.

Electropolymerization of Metal Clusters Establishing a Versatile Platform for Enhanced Catalysis Performance

Cai, Jinmeng,Gong, Chun-Hua,Han, Zhen,Li, Si,Li, Yao,Mak, Thomas C. W.,Wang, Qian-You,Wang, Shan,Wang, Yi-Man,Zang, Shuang-Quan

supporting information, (2022/01/20)

Atomically precise metal clusters are attractive as highly efficient catalysts, but suffer from continuous efficiency deactivation in the catalytic process. Here, we report the development of an efficient strategy that enhances catalytic performance by electropolymerization (EP) of metal clusters into hybrid materials. Based on carbazole ligand protection, three polymerized metal-cluster hybrid materials, namely Poly-Cu14cba, Poly-Cu6Au6cbz and Poly-Cu6Ag4cbz, were prepared. Compared with isolated metal clusters, metal clusters immobilizing on a biscarbazole network after EP significantly improved their electron-transfer ability and long-term recyclability, resulting in higher catalytic performance. As a proof-of-concept, Poly-Cu14cba was evaluated as an electrocatalyst for reducing nitrate (NO3?) to ammonia (NH3), which exhibited ≈4-fold NH3 yield rate and ≈2-fold Faraday efficiency enhancement compared to that of Cu14cba with good durability. Similarly, Poly-Cu6Au6cbz showed 10 times higher photocatalytic efficiency towards chemical warfare simulants degradation than the cluster counterpart.

Mechanism of Photoredox-Initiated C-C and C-N Bond Formation by Arylation of IPrAu(I)-CF3 and IPrAu(I)-Succinimide

Kim, Suhong,Toste, F. Dean

supporting information, p. 4308 - 4315 (2019/01/25)

Herein, we report on the photoredox-initiated gold-mediated C(sp2)-CF3 and C(sp2)-N coupling reactions. By adopting gold as a platform for probing metallaphotoredox catalysis, we demonstrate that cationic gold(III) complexes are the key intermediates of the C-C and C-N coupling reactions. The high-valent gold(III) intermediates are accessed by virtue of photoredox catalysis through a radical chain process. In addition, the bond-forming step of the coupling reactions is the reductive elimination from cationic gold(III) intermediates, which is supported by isolation and crystallographic characterization of key Au(III) intermediates.

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