54530-10-8

Basic information

• Product Name: 5-methyl-5-azahomoadamantan-4-one
• CAS NO: 54530-10-8
• Molecular Weight: 179.262
• Mol File: 54530-10-8.mol

Chemical Properties

• CAS DataBase Reference: 5-methyl-5-azahomoadamantan-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 5-methyl-5-azahomoadamantan-4-one(54530-10-8)
• EPA Substance Registry System: 5-methyl-5-azahomoadamantan-4-one(54530-10-8)

Safety Data

• Hazardous Substances Data: 54530-10-8(Hazardous Substances Data)

Upstream product

• 57777-70-5 α,α-adamantylidene-N-methyl nitrone 
• 31556-14-6 5-methoxy-4-azatricyclo[4.3.1.1^3,8]undec-4-ene 
• 22607-75-6 4-azatricyclo<4.3.1.1.^3,8>undecan-5-one 
• 54530-08-4 2-methylspiro3,7>decane> 

Relevant articles and documents

Interaction of 5-methoxy-4-azatricyclo[4.3.1.13,8]-undec-4-ene with nitrogen-containing nucleophiles

The interaction of 5-methoxy-4-azatricyclo[4.3.1.13,8]undec-4- ene with acid hydrazides has been studied. It has been established that its reaction with methoxycarbonylhydrazine leads to the formation of 6,7,8,9,10,11-hexahydro-5H-5,9:7,11-dimethano[1,2,4]triazolo[4,3-a]azocin-3-one. Special features of the alkylation of this substrate under various conditions have been studied.

Cyclic and acyclic amidines and pharmaceutical compositions containing them for use as progesterone receptor binning agents

Disclosed are cyclic and acyclic amidines, pharmaceutical compositions containing such amidines, and their use in treating or preventing progesterone receptor mediated diseases or conditions, such as osteopenia and osteoporosis.

REACTION OF CHLOROSULFONYL ISOCYANATE WITH NITRONES: AN EFFICIENT METHOD FOR THE SYNTHESIS OF CYCLIC ENAMIDES AND 2H-PYRROLES

Reaction of chlorosulfonyl isocyanate (CSI) with nitrones (derived from cyclic conjugated ketones), 1-7 and 3,4-dihydro-2H-pyrrole-1-oxides, 15a-f, has been studied.Nitrones, 1-7, react with CSI to form the enamides, 8, 10-14, and the cyclic amide, 9, in

SYNTHESIS AND TRANSFORMATIONS OF OXAZIRIDINES. ADAMANTANE-2-SPIRO-3'-OXAZIRIDINE AND ITS N-ALKYL DERIVATIVES

Unsubstituted and N-substituted adamantane-2-spiro-3'-oxaziridine were synthesized by the oxidation of Schiff bases, obtained from adamantanone and alkyl(aryl)amines, with peroxyacetic acid.The thermal rearrangement of the N-substituted derivatives leads to N-substituted 5-azahomoadamantan-4-ones, while fragmentation under the influence of Fe(II) ions leads to derivatives of bicyclononane in the form of N-substituted amides.Adamantane-2-spiro-3'-oxaziridine gives different transformation products, i.e., adamantanone in the first case and 5-azahomoadamantan-4-one in the second.