Epicamphor

Base Information

Chemical Name:Epicamphor
CAS No.:10292-98-5
Molecular Formula:C10H16 O
Molecular Weight:152.236
Hs Code.:
UNII:5OQW8QWT24
DSSTox Substance ID:DTXSID201030256
Nikkaji Number:J37.996D
Wikidata:Q27262657
Mol file:10292-98-5.mol

Synonyms:Epicamphor;10292-98-5;5OQW8QWT24;(1S,4S)-4,7,7-trimethylbicyclo[2.2.1]heptan-2-one;(-)-.beta.-Camphor;3-Bornanone, (1S,4S)-(-)-;(-)-epicamphor;Bicyclo(2.2.1)heptan-2-one, 4,7,7-trimethyl-, (1S)-;UNII-5OQW8QWT24;EPICAMPHOR, (-)-;(1S)-4,7,7-trimethylbicyclo(2.2.1)heptan-2-one;DTXSID201030256;Q27262657;BICYCLO(2.2.1)HEPTAN-2-ONE, 4,7,7-TRIMETHYL-, (1S,4S)-

Suppliers and Price of Epicamphor

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 8 raw suppliers

Chemical Property of Epicamphor

Chemical Property:

Vapor Pressure:0.168mmHg at 25°C
Melting Point:186.5°C
Refractive Index:1.4752 (estimate)
Boiling Point:213°Cat760mmHg
Flash Point:69.3°C
PSA：17.07000
Density:0.982g/cm³
LogP:2.40170
XLogP3:2.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:152.120115130
Heavy Atom Count:11
Complexity:217

Purity/Quality:: 98%,99%, ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1(C2CCC1(CC2=O)C)C
Isomeric SMILES:C[C@@]12CC[C@@H](C1(C)C)C(=O)C2

Technology Process of Epicamphor

There total 16 articles about Epicamphor which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 464-17-5,18383-34-1,2437-75-4
(-)-bornylene

: 464-49-3,68546-28-1
(1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one

: 10292-98-5
epicamphor

Guidance literature:: With potassium permanganate; sodium amalgam; mercury(II) diacetate; Multistep reaction; 1)acetic acid,room temp.;2)ether;;

Reference yield:

: 464-49-3,68546-28-1
(1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one

: 10292-98-5
epicamphor

Guidance literature:: With morpholine; sulfur; at 95 - 97 ℃; for 25h;

Reference yield:

: 30462-53-4
(1R,2S,4R)-2-Chloro-1,7,7-trimethyl-bicyclo[2.2.1]heptane

: 10292-98-5
epicamphor

Guidance literature:: Multi-step reaction with 2 steps

1: 50 percent / Potassium cyclohexyl oxide / 10 h / Heating; Cyclohexanol as solvent

2: 1)mercuric acetate 2)sodium amalgam 3)potassium permanganate / 1)acetic acid,room temp.;2)ether;

With potassium permanganate; sodium amalgam; mercury(II) diacetate; potassium cyclohexanolate;