4860-18-8

Usage

Explanation

The compound is formed by combining 1-butanethiol with copper(I) salt.

Explanation

The molecular formula represents the combination of 1-butanethiol (C4H9SH) and copper(I) (Cu+).

Explanation

The appearance of the compound is not specified, but it is likely to be a solid or liquid based on the properties of the constituent compounds.

Explanation

1-butanethiol is commonly used as a solvent in various chemical processes.

Explanation

1-butanethiol is utilized in the synthesis of certain pesticides.

Explanation

Copper(I) salts are employed in a range of industrial applications.

Explanation

Copper(I) salts serve as catalysts to facilitate specific reactions in organic chemistry.

Explanation

The compound may have potential applications in both chemistry and industry due to the properties of its constituent compounds.

Explanation

The properties and potential uses of 1-Butanethiol, Copper(I) Salt are of interest to those in the fields of research and industry.

Appearance

Unknown (likely a solid or liquid)

Solvent

Used as a solvent

Pesticide Production

Used in the production of pesticides

Industrial Applications

Used in various industrial processes

Catalysts

Used as catalysts in organic synthesis

Potential Applications

Fields of chemistry and industry

Research Interest

Researchers and industry professionals

Upstream product

• 109-79-5 n-butanethiol 
• 12775-96-1 copper 

Downstream Products

• 118464-39-4 1,2-Bis(n-butylthio)-4,5-dimethoxybenzene 
• 94612-88-1 3,4-bis(n-butylsulfenyl)-N,N-dimethylaniline 
• 136719-97-6 1-butylthio-4-(1'-methylpentyloxy)benzene 
• 94612-89-2 bis(n-butylsulfenyl)bis(N,N-dimethylamino)benzene 
• 96818-62-1 bis(n-butylsulfenyl)(N,N-dimethylamino)methylbenzene 
• 33288-22-1 C₆F₅S(n-C₄H₉) 
• 60628-11-7 4-butylsulfanyl-1-methyl-3,5-diphenyl-1H-pyrazole 
• 98606-97-4 (E)-2,3-Bis-butylsulfanyl-3-methylsulfanyl-1-phenyl-propenone 
• 98606-98-5 (Z)-2,3-Bis-butylsulfanyl-3-methylsulfanyl-1-phenyl-propenone 
• 157458-10-1 2,3-bis(n-butylthio)-4-hydroxy-5-methoxybenzaldehyde 

Relevant academic research and scientific papers

The direct electrochemical synthesis of thiolato complexes of copper, silver, and gold; the molecular structure of 2*CH3CN

The electrochemical oxidation of anodic copper or silver (= M) into non-aqueous solutions of RSH (R = alkyl, axyl) gives MISR as insoluble materials in high yield.In the presence of 1,10-phenanthroline (= L), the products are MISR*phen for M = Cu, but not Ag.Gold resists oxidation under such conditions, and AuISR (R = n-C4H9, C6H5) was obtained in only poor yield.The crystal structure of the solvated dimeric adduct 2*CH3CN is triclinic, with a = 10.682(3) Angstroem, b = 11.729(4) Angstroem, c = 15.608(5) Angstroem, α = 76.87(2) deg, β = 76.35(2) deg, γ = 68.07(2) deg, V = 1742(1) Angstroem3, Z = 2 and space group P1.The structure is based on a folded Cu2S2 ring with an unusually short Cu-Cu distance of 2.613(3) Angstroem.Each copper atom has CuS2N2 pseudo-tetrahedral stereochemistry, with Cu-S = 2.337 Angstroem (av) and Cu-N = 2.10 Angstroem (av).

The Preparation and Crystal Structure of the Unusual Copper-Sulphur Cage Complex Cu8(SC5H11)4(S2CSC5H11)4

The electrochemical oxidation of anodic copper in an acetonitrile solution of RSH (R = Ph, C10H7, CPh3, C6F4H, o-MeC6H4, CMe2Et) yields CuSR; treatment of CuSCMe2Et with CS2 produces Cu8(SR)4(S2CSR)4, whose structure is based on an unusual Cu8S12 cage.