79802-79-2

Basic information

• Product Name: Cyclohexanol, 1,3,3-trimethyl-
• CAS NO: 79802-79-2
• Molecular Formula: C9H18O
• Molecular Weight: 142.241
• Mol File: 79802-79-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Cyclohexanol, 1,3,3-trimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanol, 1,3,3-trimethyl-(79802-79-2)
• EPA Substance Registry System: Cyclohexanol, 1,3,3-trimethyl-(79802-79-2)

Safety Data

• Hazardous Substances Data: 79802-79-2(Hazardous Substances Data)

Upstream product

• 917-64-6 methyl magnesium iodide 
• 2979-19-3 3,3-dimethylcyclohexanone 
• 126-81-8 dimedone 
• 767-12-4 3,3-dimethylcyclohexanol 
• 1193-18-6 3-methylcyclohexen-2-one 
• 17123-68-1 4,4-dimethylhept-6-en-2-one 
• 37779-25-2 1,5,5-trimethylcyclohex-2-ene-1-ol 
• 917-54-4 methyllithium 
• 141-79-7 4-methyl-pent-3-en-2-one 

Downstream Products

• 3073-66-3 1,1,3-trimethylcyclohexane 
• 503-46-8 1,5,5-trimethylcyclohexene 
• 848679-93-6 1-bromo-1,3,3-trimethyl-cyclohexane 
• 968-91-2 4-nitro-peroxybenzoic acid 1,3,3-trimethyl-cyclohexyl ester 
• 39872-57-6 Isodamascone 
• 68826-42-6 1-(2,4,4-trimethyl-2-cyclohexen-1-yl)-ethanone 
• 503-47-9 1,3,3-trimethyl-1-cyclohexene 
• 219810-97-6 1-azido-1,3,3-trimethyl-cyclohexane 
• 935-55-7 1,3,3-trimethyl-cyclohexyl hydroperoxide 
• 935-53-5 1,3-Dimethyl-3-brommethyl-cyclohexan-1-ol 

Relevant articles and documents

Facile synthesis of isodamascone and its analogs

Synthesis of isodamascone and its analogs, the commercially important aroma compounds, have been accomplished from the readily available 1,5,5-trimethyl-2-cyclohexen-1-ol via a short, facile, and simple sequence of reactions in excellent yield. Copyright Taylor & Francis Group, LLC.

Synthesis and structure-affinity relationships of 1,3,5-alkylsubstituted cyclohexylamines binding at NMDA receptor PCP site

A series of 1,3,5-alkylsubstituted cyclohexylamines 2 were synthesized as ligands for the N-methyl-D-aspartate (NMDA) receptor phencyclidine (PCP) binding site. Pure diastereomers with defined configuration of amino group 2- ax and 2-eq were obtained. The optimal size of 1,3,5-substituents was determined for cyclohexylamines 2 with an equatorial amino group in the lowest energy conformation using Hansch analysis. According to the data, the lipophilic part of cyclohexylamines 2 does not discriminate between hydrophobic regions of the PCP binding site but rather recognizes this site as a whole lipophilic pocket. (C) 2000 Editions scientifiques et medicales Elsevier SAS.