(cyclohexylisocyanide)gold(I) chloride

Base Information

Chemical Name:(cyclohexylisocyanide)gold(I) chloride
CAS No.:43067-26-1
Molecular Formula:C₇H₁₁AuClN
Molecular Weight:341.591
Hs Code.:

Synonyms:(cyclohexylisocyanide)gold(I) chloride

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (cyclohexylisocyanide)gold(I) chloride

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Technology Process of (cyclohexylisocyanide)gold(I) chloride

There total 5 articles about (cyclohexylisocyanide)gold(I) chloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 99.0%

: 39929-21-0
(tetrahydrothiophene)gold(I) chloride

: 931-53-3
Cyclohexyl isocyanide

: 43067-26-1
(cyclohexylisocyanide)gold(I) chloride

Guidance literature:: In dichloromethane; Au complex reacted with ligand in CH2Cl2 at room temp.; according to A. S. K. Hashmi et al., Adv. Synth. Catal., 2010, 352, 3001; solvent evapd.;
DOI:10.1021/om2008919

Reference yield: 90.0%

: 931-53-3
Cyclohexyl isocyanide

: 29892-37-3
chloro(dimethylsulfide) gold(I)

: 43067-26-1
(cyclohexylisocyanide)gold(I) chloride

Guidance literature:: In dichloromethane; under N2; to the CH2Cl2 soln. of Au-contg. compd. (1.90 mmol) was added equimolar or excess amt. of cyclohexyl isonitrile; elem. anal.;
DOI:10.1021/ic0341946

Reference yield:

: 931-53-3
Cyclohexyl isocyanide

: 28587-97-5,635727-68-3
gold(III) chloride hydrate

: 43067-26-1
(cyclohexylisocyanide)gold(I) chloride

Guidance literature:: In water; cyclohexyl isonitrile (3.2 mmol) was added to an aq. soln. of Au-contg. compd. (1 mmol); a yellow solid was formed; the soln. was stirred; some of the solid dissolved and a brown solid formed; stirring for 30 min; the soln. was filtered; the soln. was allowed to stand for 2 h; the solid was collected by filtration and dried under vac.;
DOI:10.1021/ic0341946