DCPD-OH CAS#: 3385-61-3; ChemWhat Code: 355394

IdentificationPhysical DataSpectra
Route of Synthesis (ROS)Safety and HazardsOther Data

Identification

Product NameDCPD-OH
IUPAC Nametricyclo[5.2.1.02,6]dec-3-en-8-ol
Molecular StructureStructure of DCPD-OH CAS 3385-61-3
CAS Registry Number 3385-61-3
EINECS Number222-197-4
MDL NumberNo data available
Beilstein Registry NumberNo data available
Synonymstricyclo<5,2,1,0 2,6>-3-decene-8-olhydroxydicyclopentadieneTricyclo<5.2.1.0>dec-3-en-8-ol2-Oxydihydrodicyclopentadientricyclo[5.2.1.02,6 ]deca-3-en-8-ol
Molecular FormulaC10H14O
Molecular Weight150.221
InChIInChI=1S/C10H14O/c11-10-5-6-4-9(10)8-3-1-2-7(6)8/h1-2,6-11H,3-5H2
InChI KeyHIPPBUJQSIICJN-UHFFFAOYSA-N
Canonical SMILESC1C=CC2C1C3CC2CC3O
Patent Information
Patent IDTitlePublication Date
US2007/49767Method of making carbonyl compounds 2007
US4916255Method for production of methacrylate ester1990

Physical Data

AppearanceColorless or light yellow transparent liquid
SolubilityNo data available
Flash PointNo data available
Refractive indexNo data available
SensitivityNo data available
Refractive IndexWavelength (Refractive Index), nmTemperature (Refractive Index), °C
1.526258920
1.52458925
1.525558920
Boiling Point, °CPressure (Boiling Point), Torr
1179
101 – 1022
79 – 810.4
Density, g·cm-3Reference Temperature, °CMeasurement Temperature, °C
1.0779425

Spectra

Description (NMR Spectroscopy)Nucleus (NMR Spectroscopy)Solvents (NMR Spectroscopy)Temperature (NMR Spectroscopy), °C Frequency (NMR Spectroscopy), MHz
Chemical shifts1Hchloroform-d125600
Chemical shifts13Cchloroform-d125150

Route of Synthesis (ROS)

Route of Synthesis (ROS) of DCPD-OH CAS#: 3385-61-3
ConditionsYield
With methanol; potassium carbonate at 20℃; for 2h;

Experimental Procedure
1.2; 2.2; 3.2; 4.2; 5.2; 6.2; 7.2; 8.2
General procedure: (2) 10.5 g of tricyclodecenyl trifluoroacetate was dissolved in 100 mL of methanol,11.7 g of K2CO3 was added and stirred at room temperature for 2 h. Concentrate the methanol to dryness,Add 50 mL of water, extract with dichloromethane (50 mL x 2), and combine the organic phases.Dilute hydrochloric acid (1mol/L) to neutral, washed with saturated sodium chloride solution,Dry over anhydrous sodium sulfate,Concentration gave 5.8 g of tricyclic terpene alcohol as a colorless oil with a yield of 94% and a GC content of 97.5%.		95.6%

Safety and Hazards

Pictogram(s)exclamation-mark
SignalWarning
GHS Hazard StatementsH315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
H412 (100%): Harmful to aquatic life with long lasting effects [Hazardous to the aquatic environment, long-term hazard]
Information may vary between notifications depending on impurities, additives, and other factors.
Precautionary Statement CodesP264, P264+P265, P273, P280, P302+P352, P305+P351+P338, P321, P332+P317, P337+P317, P362+P364, and P501
(The corresponding statement to each P-code can be found at the GHS Classification page.)

Other Data

TransportationNONH for all modes of transport
Under the room temperature and away from light
HS CodeNo data available
StorageUnder the room temperature and away from light
Shelf Life1 year
Market PriceUSD
Druglikeness
Lipinski rules component
Molecular Weight150.221
logP1.95
HBA1
HBD1
Matching Lipinski Rules4
Veber rules component
Polar Surface Area (PSA)20.23
Rotatable Bond (RotB)0
Matching Veber Rules2
Use Pattern
DCPD-OH CAS 3385-61-3 used in resin synthesis and polyurethane.

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