15904-95-7

Basic information

• Product Name: TRICYCLO[5.2.1.0(2,6)]DECAN-8-OL
• Synonyms: TRICYCLO[5.2.1.0(2,6)]DECAN-8-OL;TIMTEC-BB SBB000113;4,7-Methanoindan-5-ol, hexahydro-;4,7-Methanoinden-5-ol, perhydro-;Ai3-12158;Einecs 236-455-9;Nsc 22466
• CAS NO: 15904-95-7
• Molecular Formula: C10H16O
• Molecular Weight: 152.23
• Mol File: 15904-95-7.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: TRICYCLO[5.2.1.0(2,6)]DECAN-8-OL(CAS DataBase Reference)
• NIST Chemistry Reference: TRICYCLO[5.2.1.0(2,6)]DECAN-8-OL(15904-95-7)
• EPA Substance Registry System: TRICYCLO[5.2.1.0(2,6)]DECAN-8-OL(15904-95-7)

Safety Data

• Hazardous Substances Data: 15904-95-7(Hazardous Substances Data)

Upstream product

• 3385-61-3 tricyclo<5,2,1,0 2,6>-3-decene-8-ol 
• 77-73-6 bi(cyclopentadiene) 
• 13380-94-4 octahydro-4,7-methano-inden-5-one 
• 1755-01-7 endo-Dicyclopentadien 
• 2826-19-9 (3aR^*,4S^*,7R^*,7aS^*)-2,3,3a,4,7,7a-hexahydro-4,7-methano-1H-indene 
• 84402-51-7 syn-8-Bromoctahydro-endo-4,7-methanoinden-exo-5-ol 
• 7664-93-9 sulfuric acid 
• 65470-96-4 (1R^*,3aS^*,4R^*,7S^*,7aR^*)-2,3,4a,4,7,7a-hexahydro-4,7-methano-1H-inden-1-ol 
• 22981-84-6 (3aS^*,4R^*,7S^*,7aR^*)-2,3,4a,4,7,7a-hexahydro-4,7-methano-1H-inden-1-one 
• 125877-73-8 (1R^*,3aS^*,4R^*,7S^*,7aR^*)-2,3,3a,4,7,7a-hexahydro-1-((methylsulfonyl)oxy)-4,7-methano-1H-indene 
• 542-92-7 cyclopenta-1,3-diene 
• 120-92-3 cyclopentanone 
• 142-29-0 cyclopentene 
• 2825-83-4 (3aR,4R,7S,7aS)-octahydro-1H-4,7-methanoindene 

Downstream Products

• 1096688-05-9 (3aS,4S,5R,7R,7aS)-octahydro-1H-4,7-methanoinden-5-ol 

Relevant articles and documents

What Is the True Structure of D609, a Widely Used Lipid Related Enzyme Inhibitor?

(Chemical Equation Presented) D609 (1) has been used as a lipid-related enzyme inhibitor during the past three decades. Although it has eight possible stereoisomers, no systematic research considering its chirality has been performed. In this paper, eight possible chiral alcohols as direct precursors of D609 were synthesized, and their stereochemistries were elucidated by a vibrational circular dichroism (VCD) technique. Phosphatidylcholine-specific phospholipase C and sphingomyelin synthase inhibition assays of these isomers showed considerable differences in their activities.

Glass transition temperature enhancement of PMMA through copolymerization with PMAAM and PTCM mediated by hydrogen bonding

A series of poly(methyl methacrylate-co-methacrylamide-co-tricyclodecyl methacrylate) (PMMA-co-PMAAM-co-PTCM) copolymers possessing high glass transition temperatures and high transparency are prepared. By incorporating the aliphatic tricyclodecyl methacrylate moiety into the PMMA-co-PMAA main chain results in high glass transition temperature and high transparency of PMMA-based polymeric material. The TCM content affects the fraction of hydrogen bonding in these terpolymers, small content of TCM does not sacrifice the fraction of hydrogen-bonded association in and does not cause Tg decrease. The extent of free amide group plays the major role in dictating moisture absorption of terpolymers. The incorporation of TCM significantly reduces the moisture absorption of terpolymers due to its hydrophobic and bulky tricyclodecyl group. In addition, the TCM plays the role of inert diluent to convert portion of the strong self-associated hydrogen bonded amide groups into inter-associated hydrogen bonding between carbonyl groups of ester units and MAAM.

Synthesis and Reactions of Tricyclic Monocarboxylic Acid Esters

A convenient and efficient method for preparing tricyclic esters has been developed on the basis of addition of C1-C3 monocarboxylic acids to tricyclo2,6>deca-3,8-diene and its dimethyl derivatives in the presence of p-toluenesulfonic acid.The orientation of the ester group in the products has been determined.Some reactions of the resulting esters have been studied, and their possible applications have been proposed.