10035-86-6

Basic information

• Product Name: Cyclohexanecarbothioic acid, S-ethyl ester
• CAS NO: 10035-86-6
• Molecular Formula: C9H16OS
• Molecular Weight: 172.291
• Mol File: 10035-86-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Cyclohexanecarbothioic acid, S-ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanecarbothioic acid, S-ethyl ester(10035-86-6)
• EPA Substance Registry System: Cyclohexanecarbothioic acid, S-ethyl ester(10035-86-6)

Safety Data

• Hazardous Substances Data: 10035-86-6(Hazardous Substances Data)

Upstream product

• 124555-76-6 Cyclohex-1-enecarbothioic acid S-ethyl ester 
• 636-82-8 cyclohexene-1-carboxylic acid 
• 36432-89-0 C₁₄H₁₉N₃O₂S 
• 95633-73-1 2-cyclohexylcarbonyl-1-methyl-1H-imidazole 
• 2528-61-2 Heptanoic acid chloride 
• 70974-42-4 1-(pyrrolidin-1-yl)heptan-1-one 
• 95633-74-2 2-heptanoyl-1-methyl-1H-imidazole 
• 106-73-0 methyl heptanoate 
• 111-14-8 oenanthic acid 
• 2719-27-9 cyclohexanylcarbonyl chloride 
• 75-08-1 ethanethiol 
• 98-89-5 Cyclohexanecarboxylic acid 

Downstream Products

• 16076-62-3 ethyl 6-cyclohexyl-6-oxohexanoate 
• 15971-95-6 4-cyclohexyl-4-oxo-butyric acid 
• 17615-04-2 Triphenyl-(hexahydrobenzoyl-methoxycarbonyl-methyl-methylen)-phosphoran 
• 116237-11-7 (1S*,5S*,7R*,8R*)-8-(3-cyclohexyl-3-hydroxy-1-propenyl)-7-hydroxy-N-m-methoxycarbonylbenzoyl-3-azabicyclo<3.3.0>octane 
• 116237-13-9 (1S*,5S*,7R*,8R*)-N-m-carboxybenzoyl-8-(3-cyclohexyl-3-oxo-1-propenyl)-7-hydroxy-3-azabicyclo<3.3.0>octane 
• 116237-10-6 (1S*,5S*,7R*,8R*)-8-(3-cyclohexyl-3-oxo-1-propenyl)-7-hydroxy-N-m-methoxycarbonylbenzoyl-3-azabicyclo<3.3.0>octane 
• 1674-37-9 n-octanophenone 
• 19844-05-4 Ethylsulfanylmethyl-cyclohexane 
• 100-49-2 cyclohexylmethyl alcohol 
• 17615-02-0 1-cyclohexyl-2-(triphenyl-λ⁵-phosphanylidene)ethan-1-one 
• 701-97-3 cyclohexanepropionic acid 

Relevant articles and documents

GENERATION OF AN ACTIVE ACYL SPECIES FROM STABLE 1-METHYL-2-ACYL-1H-IMIDAZOLES

1-Methyl-2-(1'-cyano-1'-trimethylsilyloxy)alkyl-1H-imidazoles (2) were easily prepared from the corresponding stable carbonyl compounds, 1-methyl-2-acyl-1H-imidazoles (1).When the quarternary salts of 2 were treated with various nucleophiles, reactive acyl species, which was presumed to be acylcyanide (12), was generated in situ under C-C bond fission to result in producing the corresponding acylated compounds (5-10) in good yields.

THIOL ESTER IN ORGANIC SYNTHESIS XV. REDUCTION WITH TETRABUTYLAMMONIUM BOROHYDRIDE

Treatment of thiol ester with tetrabutylammmonium borohydride in refluxing chloroform gave rise to the corresponding alcohols.