118832-55-6

Basic information

• Product Name: 5-Bromo-6-cyclohexylmethyl-3-isopropyl-tetrahydro-pyran-2-one
• Synonyms: 5-Bromo-6-cyclohexylmethyl-3-isopropyl-tetrahydro-pyran-2-one
• CAS NO: 118832-55-6
• Molecular Weight: 317.266
• Mol File: 118832-55-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 5-Bromo-6-cyclohexylmethyl-3-isopropyl-tetrahydro-pyran-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Bromo-6-cyclohexylmethyl-3-isopropyl-tetrahydro-pyran-2-one(118832-55-6)
• EPA Substance Registry System: 5-Bromo-6-cyclohexylmethyl-3-isopropyl-tetrahydro-pyran-2-one(118832-55-6)

Safety Data

• Hazardous Substances Data: 118832-55-6(Hazardous Substances Data)

Upstream product

• 108-12-3 isopentanoyl chloride 
• 118832-50-1 (4'E,4S,2'S)-N-<6'-cyclohexyl-2'-(1-methylethyl)-4'-hexenoyl>-4-(1-methylethyl)-2-oxazolidinone 
• 96930-24-4 (4S)-N-(3-methylbutanoyl)-4-(1-methylethyl)-2-oxazolidinone 
• 118917-71-8 (4E,2S)-6-cyclohexyl-2-(1-methylethyl)-4-hexenoic acid 
• 196706-22-6 (E)-6-cyclohexyl-2-(1-methylethyl)-4-hexenoic acid 
• 118832-46-5 2-Isopropyl-malonic acid 1-cyclohexylmethyl-allyl ester ethyl ester 
• 118832-47-6 (E)-6-Cyclohexyl-2-isopropyl-hex-4-enoic acid ethyl ester 
• 118917-67-2 (E)-(S)-6-Cyclohexyl-2-isopropyl-hex-4-enoyl chloride 
• 759-36-4 diethyl isopropylmalonate 
• 192060-34-7 N-[(1S,2S)-2-hydroxy-1-methyl-2-phenylethyl]-3-N-dimethylbutyramide 
• 5664-21-1 cyclohexylacetaldehyde 
• 118832-49-8 (E)-4-bromo-1-cyclohexyl-2-butene 
• 118040-79-2 1-cyclohexylbut-3-en-2-ol 
• 196706-16-8 (E)-(S)-6-Cyclohexyl-2-isopropyl-hex-4-enoic acid ((1S,2S)-2-hydroxy-1-methyl-2-phenyl-ethyl)-methyl-amide 

Relevant articles and documents

Formal, Stereoselective Synthesis of Hydroxyethylene Dipeptide Isosteres Utilizing Pseudoephedrine Amides

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A Versatile and Stereocontrolled Synthesis of Hydroxyethylene Dipeptide Isosteres

An asymmetric synthesis of the hydroxyethylene dipeptide isostere unit 1 is described.The synthesis provides excellent stereocontrol over all three chiral centers and is amenable to variation of substituents R1 and R2.Key intermediat