17773-63-6

Basic information

• Product Name: Methanone, cyclohexylcyclopentyl-
• CAS NO: 17773-63-6
• Molecular Formula: C12H20O
• Molecular Weight: 180.29
• Mol File: 17773-63-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Methanone, cyclohexylcyclopentyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanone, cyclohexylcyclopentyl-(17773-63-6)
• EPA Substance Registry System: Methanone, cyclohexylcyclopentyl-(17773-63-6)

Safety Data

• Hazardous Substances Data: 17773-63-6(Hazardous Substances Data)

Upstream product

• 142-29-0 cyclopentene 
• 2719-27-9 cyclohexanylcarbonyl chloride 
• 3282-54-0 1-cyclohexyl-1-cyclohexene 
• 98-89-5 Cyclohexanecarboxylic acid 
• 2043-61-0 cyclohexanecarbaldehyde 
• 32916-51-1 cyclopentylmagnesium chloride 
• 931-51-1 cyclohexylmagnesiumchloride 
• 4832-52-4 tris(phenylthio)methane 
• 872267-21-5 cyclohexyl(cyclopentyl)methanol 
• 1066-30-4 chromium(lll) acetate 
• 4441-56-9 cyclohexylboronic acid 
• 4524-93-0 Cyclopentanecarboxylic acid chloride 
• 446065-11-8 cyclohexyltrifluoro-λ⁴-borane potassium salt 
• 286-20-4 cyclohexane-1,2-epoxide 

Downstream Products

• 4431-89-4 (cyclopentylmethyl)cyclohexane 

Relevant articles and documents

Nickel-Catalyzed Cross-Coupling of Alkyl Carboxylic Acid Derivatives with Pyridinium Salts via C-N Bond Cleavage

The electrophile-electrophile cross-coupling of carboxylic acid derivatives and alkylpyridinium salts via C-N bond cleavage is developed. The method is distinguished by its simplicity and steers us through a variety of functionalized ketones in good to excellent yields. Besides acid chlorides, carboxylic acids were also employed as acylating agents, which enabled us to incorporate acid-sensitive functional groups such as MOM, BOC, and acetal. Control experiments with TEMPO revealed a radical pathway.

LITHIUM TRIS(PHENYLTHIO)METHANE FOR THE HOMOLOGATION OF TRIALKYLBORANES: CONVENIENT SYNTHESES OF KETONES AND t-CARBINOLS

Lithium tris(phenylthio)methane is a readily available, cheap reagent for the production of ketones and t-carbinols from trialkylboranes.The scope and limitations of the reactions are indicated as are some of its unique features.