32166-40-8

Basic information

• Product Name: cis-1-decalone
• Synonyms: cis-1-decalone
• CAS NO: 32166-40-8
• Molecular Weight: 152.236
• Mol File: 32166-40-8.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: cis-1-decalone(CAS DataBase Reference)
• NIST Chemistry Reference: cis-1-decalone(32166-40-8)
• EPA Substance Registry System: cis-1-decalone(32166-40-8)

Safety Data

• Hazardous Substances Data: 32166-40-8(Hazardous Substances Data)

Upstream product

• 493-01-6 cis-decalin 
• 18631-96-4 3,4,5,6,7,8-hexahydro-2H-naphthalen-1-one 
• 74-88-4 methyl iodide 
• 155511-10-7 (E)-10-Iododeca-1,6-dien-3-one 
• 115033-78-8 Se-phenyl 4-(1-cyclohexenyl)butaneselenoate 
• 74056-05-6 2-(4-Bromobutyl)-2-cyclohexen-1-one 
• 130660-16-1 3-(4-Iodo-butyl)-cyclohex-2-enone 

Downstream Products

• 2529-03-5 (1RS,4aRS,8aSR)-decahydronaphthalen-1-ol 
• 17429-48-0 2-benzyliden-octahydro-naphthalen-1-one 
• 17429-44-6 (+/-)-4-oxo-4ar-methyl-3-(benzylidene-(seqtrans))-(8acH)-decalin 
• 17429-44-6 (+/-)-4-oxo-4ar-methyl-3-(benzylidene-(seqtrans))-(8atH)-decalin 
• 2384-68-1 trans-Octahydro-naphtalin-1-on-semicarbazon 
• 529-32-8 (4ar,8ac)-decahydro-naphthalen-1t-ol 
• 529-32-8 trans,trans-decahydro-1-naphthol 
• 101787-68-2 (+/-)-2-((E)-4-methoxy-benzyliden)-(4ar,8at)-octahydro-naphthalen-1-one 
• 17429-48-0 (+/-)-2-((E)-benzyliden)-(4ar,8at)-octahydro-naphthalen-1-one 
• 17429-49-1 (+/-)-2-((E)-4-chloro-benzyliden)-(4ar,8at)-octahydro-naphthalen-1-one 
• 2384-68-1 (+/-)-1-Semicarbazono-cis-decalin 
• 103263-24-7 3-(2-carboxy-cyclohexyl)-propionic acid 
• 21370-71-8 trans-1-decalone 
• 4832-16-0 1-decalone 

Relevant articles and documents

Mild and selective oxyfunctionalization of hydrocarbons by perfluorodialkyloxaziridines

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An iron catalyst for oxidation of alkyl C-H bonds showing enhanced selectivity for methylenic sites

Many are called but few are chosen: A nonheme iron complex catalyzes the oxidation of alkyl C-H bonds by using H2O2 as the oxidant, showing an enhanced selectivity for secondary over tertiary C-H bonds (see scheme). Copyright

The selective functionalization of saturated hydrocarbons. Part 46. An investigation of Udenfriend's system under Gif conditions

Under Gif conditions using ascorbic acid as reductant and oxygen as oxidant in pyridine, the selectivity for secondary hydrogen functionalization is exceptional. EDTA (ethylenediamine-tetra-acetic acid) is not needed as a ligand for iron.