368875-06-3

Basic information

• Product Name: 1H-Inden-1-one,octahydro-3a-methyl-,(3aS,7aS)-(9CI)
• Synonyms: 1H-Inden-1-one,octahydro-3a-methyl-,(3aS,7aS)-(9CI)
• CAS NO: 368875-06-3
• Molecular Formula: C10H16O
• Molecular Weight: 0
• Product Categories: CYCLOPENTANE
• Mol File: 368875-06-3.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H-Inden-1-one,octahydro-3a-methyl-,(3aS,7aS)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Inden-1-one,octahydro-3a-methyl-,(3aS,7aS)-(9CI)(368875-06-3)
• EPA Substance Registry System: 1H-Inden-1-one,octahydro-3a-methyl-,(3aS,7aS)-(9CI)(368875-06-3)

Safety Data

• Hazardous Substances Data: 368875-06-3(Hazardous Substances Data)

Upstream product

• 53068-89-6 (S)-3-(1-methyl-2-oxocyclohexyl)-propionic acid methyl ester 
• 53068-89-6 (R)-(+)-2-(2'-carbomethoxyethyl)-2-methylcyclohexanone 
• 63714-74-9 3-(1-Methyl-cyclohex-2-enyl)-propionic acid methyl ester 
• 6432-30-0 2-hydroxy-6-methylbicyclo<4.4.0>decan-3-one 
• 826-56-2 4a-methyl-4,4a,5,6,7,8-hexahydro-3H-naphthalen-2-one 
• 13837-12-2 3,4,5,6,7,8-hexahydro-2(1H)-naphthalenone 
• 20990-27-6 <4.3.1>propellan-7-one 
• 144126-65-8 3-(1-methyl-2-oxocyclohexyl)propanenitrile 
• 16938-80-0 1-Oxo-3a-brommethyl-perhydroinden 
• 21378-21-2 3-methylcyclohex-2-en-1-ol 
• 71593-69-6 1-methyl-2-cyclohexen-1-acetic acid ethyl ester 

Downstream Products

• 368875-13-2 1-allyl-3α-methyloctahydroindene-1,7-diol 
• 70219-47-5 3α-methyl-2,3,3',4,5,6-hexahydroinden-1-one 
• 607680-05-7 (3aS)-3a-methyl-2,3,3a,4,5,6-hexahydroinden-1-one 

Relevant articles and documents

-

-

On the bioactive conformation of the rhodopsin chromophore: Absolute sense of twist around the 6-s-cis bond

Incubation of opsin with synthetic 6-s-locked retinoids 2a and 2b only led to pigment formation from the alpha-locked 2a, the CD spectrum of which was similar to that of native rhodopsin (Rh). This establishes that the 6-s-bond of the chromophore in rhodo

Electroorganic Chemistry. 140. Electroreductively Intra- and Intermolecular Couplings of Ketones with Nitriles

Electroreduction of γ- and δ-cyano ketones in i-PrOH with Sn cathode gave α-hydroxy ketones and their dehydroxylated ketones as the intramolecularly coupled products.Guaiazulene, (-)-valeranone, polyquinanes, dihydrojasmone, methyl dihydrojasmonate, and rosaprostol have been synthesized by utilizing this electroreductive intramolecular coupling of γ- and δ-cyano ketones in one of the key steps.Similarly, electroreduction of a mixture of ketone and nitrile gave the corresponding intermolecularly coupled product.The product obtained by the electroreductive intermolecular coupling of (+)-dihydrocarvone with acetonitrile has been found to be the precursor of an effective chiral ligand for the enantioselective addition of diethylzinc to aldehydes.