21766-50-7

Basic information

• Product Name: 1(2H)-Naphthalenone, octahydro-4-hydroxy-
• CAS NO: 21766-50-7
• Molecular Formula: C10H16O2
• Mol File: 21766-50-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1(2H)-Naphthalenone, octahydro-4-hydroxy-(CAS DataBase Reference)
• NIST Chemistry Reference: 1(2H)-Naphthalenone, octahydro-4-hydroxy-(21766-50-7)
• EPA Substance Registry System: 1(2H)-Naphthalenone, octahydro-4-hydroxy-(21766-50-7)

Safety Data

• Hazardous Substances Data: 21766-50-7(Hazardous Substances Data)

Upstream product

• 2717-36-4 cis-octahydronaphthalen-1,4-dione 
• 106-51-4 p-benzoquinone 
• 35043-92-6 cis-5,8,9,10-tetrahydronaphtho-1,4-quinone 
• 74069-53-7 (4α,4aβ,8aβ)-4-hydroxy-4a,5,8,8a-tetrahydronaphthalen-1-(4H)-one 
• 6751-42-4 trans-octahydronaphthalen-1,4-dione 
• 21766-50-7 (4α,4aβ,8aβ)-4-hydroxyoctahydronaphthalen-1(2H)-one 
• 2906-93-6 (+/-)-1,4,5,8,9,10-trans-hexahydronaphthalene-1,4-dione 
• 16786-42-8 (4aR)-(4ar,8ac)-decahydro-naphthalene-1c,4t-diol 
• 2906-95-8 (+)-(4S,9S)-4-Hydroxy-trans-Δ⁶-octalon-1 
• 1127-50-0 trans-Decalin-1α,4β-diol 
• 1127-50-0 trans-Decalin-1β,4β-diol 
• 2906-94-7 (4S,4aR,8aR)-4-Hydroxy-3,4,4a,5,8,8a-hexahydro-2H-naphthalen-1-one 
• 21766-50-7 (4aR)-4t-hydroxy-(4ar,8ac)-octahydro-naphthalen-1-one 
• 1127-50-0 (+)-(1S,4S,9R)-trans-Dekalin-1,4-diol 

Downstream Products

• 21766-50-7 (4aR)-4c-hydroxy-(4ar,8at)-octahydro-naphthalen-1-one 
• 21766-50-7 (4aR)-4t-hydroxy-(4ar,8at)-octahydro-naphthalen-1-one 
• 21766-50-7 (4α,4aβ,8aβ)-4-hydroxyoctahydronaphthalen-1(2H)-one 
• 3275-81-8 (1S,4aS,8aR)-decahydronaphthalen-1-ol 
• 101787-81-9 phenylglyoxylic acid-((4aR)-(4ar,8at)-decahydro[1t]naphthyl ester) 
• 1127-50-0 (+/-)-1c.4c-Dihydroxy-(4arH,8acH)-decalin 
• 1127-50-0 1c,4t,9c,10t-Decalindiol-(1,4) 
• 1127-50-0 1t,4c,9c,10t-Decalindiol-(1,4) 
• 52079-69-3 1c.9c.10t-α-Dekalol 

Relevant articles and documents

Spectroscopic and X-ray crystallographic evidence for electrostatic effects in 4-substituted cyclohexanone-derived hydrazones, imines, and corresponding salts

The axial conformer of several 4-substituted cyclo-hexanone hydrazone salts was found to predominate in solution. Changes in the charge of the molecule and the polarity of the solvent led to changes in the conformational preference of each molecule that were consistent with electrostatic stabilization of the axial conformer. H NMR spectroscopic analysis was utilized to determine the structure of cyclohexanone-derived substrates by comparison to conformationally restricted trans-decalone derivatives and computational models. X-ray crystallography demonstrated that the axial configuration of a pendant benzyloxy group is the preferred conformation of an iminium ion in the solid state. The structure of a neutral hydrazone was also determined to favor the axial configuration for a pendant benzyloxy group in the solid state.