6102-41-6

Basic information

• Product Name: rel-(4aS,8aS)-1,2,3,4,4a,5,8,8a-octahydronaphthalen-2-one
• CAS NO: 6102-41-6
• Molecular Weight: 150.221
• Mol File: 6102-41-6.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: rel-(4aS,8aS)-1,2,3,4,4a,5,8,8a-octahydronaphthalen-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: rel-(4aS,8aS)-1,2,3,4,4a,5,8,8a-octahydronaphthalen-2-one(6102-41-6)
• EPA Substance Registry System: rel-(4aS,8aS)-1,2,3,4,4a,5,8,8a-octahydronaphthalen-2-one(6102-41-6)

Safety Data

• Hazardous Substances Data: 6102-41-6(Hazardous Substances Data)

Upstream product

• 106-99-0 buta-1,3-diene 
• 106-51-4 p-benzoquinone 
• 930-68-7 cyclohexenone 

Downstream Products

• 111219-19-3 C₁₇H₂₂N₂O₂S 
• 1123-77-9 cis-2,3-octalin 
• 2001-50-5 trans-2,3-octalin 
• 84175-98-4 ethyl α-rel-(1S,3aS,5aS,6S,9aR)-6-<2-(tert-butyldiphenylsiloxy)ethyl>dodecahydropyrrolo<1,2-a>quinol-1-yl acetate 
• 84236-41-9 ethyl α-rel-(1R,3aS,5aS,6S,9aR)-6-<2-(tert-butyldiphenylsiloxy)ethyl>dodecahydropyrrolo<1,2-a>quinol-1-yl acetate 
• 80664-53-5 N--5-thiophenoxy-2-pyrrolidinone 
• 75685-48-2 (+/-)-gephyrotoxin 
• 84175-96-2 rel-(3aS,5aS,6S,9aR)-1(E)-(carbethoxymethylidene)-6-((2-tert-butyldiphenylsiloxy)ethyl)dodecahydropyrrolo<1,2-a>quinoline 
• 78392-02-6 2-quinol-1-yl>ethyl tert-butyldiphenylsilyl ether 
• 75685-52-8 1α,2,3,3aα,4,5,5aβ,6α,7,8,9,9aβ-dodecahydro-1-<2-<(tert-butyldiphenylsilyl)oxy>ethyl>-6-(2-hydroxyethyl)pyrrolo<1,2-a>quinoline 
• 78392-01-5 2-quinol-1-yl>ethyl tert-butyldiphenylsilyl ether 
• 78328-74-2 2-quinol-1-yl>ethyl tert-butyldiphenylsilyl ether 
• 78308-02-8 N-succinimide 
• 78308-03-9 N-succinimide 

Relevant articles and documents

Palladium-mediated transannular cyclizations of medium-ring olefinic enolsilanes

Medium-ring olefinic ketone and lactone enolsilanes were subjected to palladium(II)-mediated cycloalkenylation conditions. Diverse bicyclic ring products were obtained in moderate to good yields. The effect of olefin geometry and ring size is discussed.

A straightforward route to functionalized trans-diels-alder motifs

A sequence consisting of a Lewis acid-catalyzed Diels-Alder reaction on a 2-halocyclohexenone, followed by reductive alkylation, provides a route to trans-fused octalinones bearing angular methyl groups with functionality corresponding to that which would have been possible from a trans-directed Diels-Alder reaction.

Enzymes in organic synthesis. 37. Preparation and characterization of potential decalindione substrates of horse liver alcohol dehydrogenase

The preparations of ten decalindiones for investigation as substrates of horse liver alcohol dehydrogenase are reported.The structure characterizations include clarifications of some ambiguities in the decalin literature.