90925-16-9

Basic information

• Product Name: 7-methyl-2,3,3a,4,7,7a-hexahydro-inden-1-one
• Synonyms: 7-methyl-2,3,3a,4,7,7a-hexahydro-inden-1-one
• CAS NO: 90925-16-9
• Molecular Weight: 150.221
• Mol File: 90925-16-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 7-methyl-2,3,3a,4,7,7a-hexahydro-inden-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 7-methyl-2,3,3a,4,7,7a-hexahydro-inden-1-one(90925-16-9)
• EPA Substance Registry System: 7-methyl-2,3,3a,4,7,7a-hexahydro-inden-1-one(90925-16-9)

Safety Data

• Hazardous Substances Data: 90925-16-9(Hazardous Substances Data)

Upstream product

• 930-30-3 cyclopent-2-enone 
• 2004-70-8 1-methylbuta-1,3-diene 

Downstream Products

• 461641-22-5 5-methyl-4-[1-(toluene-4-sulfonyl)-1H-indol-3-yl]-1,9,9a,10a-tetrahydro-4H,4bH-10-oxa-4a-aza-indeno[1,2-a]indene-2-carboxylic acid ethyl ester 
• 461641-23-6 1-{4-hydroxymethyl-6-[1-(toluene-4-sulfonyl)-1H-indol-3-yl]-3,6-dihydro-2H-pyridin-1-yl}-7-methyl-indan-2-ol 
• 461641-11-2 5-methyl-4-phenyl-1,9,9a,10a-tetrahydro-4H,4bH-10-oxa-4a-aza-indeno[1,2-a]indene-2-carboxylic acid ethyl ester 
• 461641-19-0 (1S,2R)-(-)-cis-1-[(2R)-4-hydroxymethyl-2-phenyl-1,2,5,6-tetrahydropyridin-1-yl]-7-methylindan-2-ol 
• 7344-34-5 4-methyl-1H-indene 
• 39627-61-7 7-methyl-1-indanone 

Relevant articles and documents

Asymmetric synthesis of chiral 1,3-diaminopropanols: Bisoxazolidine- catalyzed C-C bond formation with α-keto amides

Three high-yielding steps lead to the formation of chiral 1,3-diaminopropanols from aliphatic and aromatic α-keto amides. In this approach, a nitroaldol reaction, which is catalyzed by Cu(SO2CF 3)2 and the bisoxazolidine ligand L1, is followed by two mild reduction reactions (see scheme). Laborious protection and deprotection steps can be avoided by using this method.

Development of highly stereoselective asymmetric 6π- azaelectrocyclization of conformationally flexible linear 1-azatrienes. From determination of multifunctional chiral amines, 7-alkyl cis-1-amino-2-indanols, to application as a new synthetic strategy: Formal synthesis of 20-epiuleine

The highly stereoselective asymmetric 6π-azaelectrocyclization was achieved as a general synthetic method based on the reaction between the (E)-3-carbonyl-2,4,6-trienal compounds and the (-)-7-alkyl-cis-l-amino-2-indanol derivatives which are effective chiral amines. The 7-alkyl-substituted 2-indanol moiety of the cyclized products was efficiently removed by the novel manganese dioxide oxidation under remarkably mild conditions, and the method was successfully applied to the formal synthesis of optically active 20-epiuleine.