exo-Norborneol

Base Information

Chemical Name:exo-Norborneol
CAS No.:29583-34-4
Molecular Formula:C₇H₁₂O
Molecular Weight:112.172
Hs Code.:
European Community (EC) Number:207-845-6
UNII:X3I1L0DS1A
DSSTox Substance ID:DTXSID7022041
Nikkaji Number:J231.879B
Wikipedia:Exo-Norborneol

Synonyms:exo-Norborneol;(1R,2R,4S)-bicyclo[2.2.1]heptan-2-ol;29583-34-4;(+)-exo-norborneol;X3I1L0DS1A;497-37-0;(1R,2R,4S)-Norbornan-2-ol;2-Norbornanol, (1R,2R)-(+)-;J231.879B;Bicyclo(2.2.1)heptan-2-ol, (1R-exo)-;(1R,2R,4S)-Bicyclo(2.2.1)heptan-2-ol;(1R,2R,4S)-Bicyclo(2.2.1)heptane-2-ol;Bicyclo(2.2.1)heptan-2-ol, (1R,2R,4S)-;exo-Norbornanol;exo-2-Norborneol;exo-2-Norbornanol;exo-Bicyclo[2.2.1]heptan-2-ol;exo-2-Norbornyl alcohol;OC1CC2CCC1C2;exo-Bicyclo(2.2.1)heptan-2-ol;EINECS 207-845-6;Bicyclo[2.2.1]heptan-2-ol, exo-;NSC 167460;AI3-51349;exo-Norborneol, (+)-;Bicyclo(2.2.1)heptan-2-ol, (1R,2R,4S)-rel-;Bicyclo[2.2.1]heptan-2-ol, (1R,2R,4S)-rel-;UNII-X3I1L0DS1A;SCHEMBL472774;DTXSID7022041;NORBORNEOL, EXO-(+)-;(1R,2R,4S)-Norbornane-2-ol;MFCD00136051;AKOS037651098;CS-15884;CS-0063194;Bicyclo[2.2.1]heptan-2-ol,(1S,2R,4R)-;D73283;(1alpha,4alpha)-Bicyclo(2.2.1)heptan-2alpha-ol;(1R*,2R*,4S*)-Bicyclo[2.2.1]heptan-2-ol;(1.ALPHA.,4.ALPHA.)-BICYCLO(2.2.1)HEPTAN-2.ALPHA.-OL

Suppliers and Price of exo-Norborneol

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 1 raw suppliers

Chemical Property of exo-Norborneol

Chemical Property:

XLogP3:1.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:112.088815002
Heavy Atom Count:8
Complexity:101

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CC2CC1CC2O
Isomeric SMILES:C1C[C@@H]2C[C@H]1C[C@H]2O

Technology Process of exo-Norborneol

There total 49 articles about exo-Norborneol 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: 100.0%

: 497-38-1,2630-41-3
(1S,4R)-bicyclo[2.2.1]heptan-2-one

: 497-36-9,497-37-0,1632-68-4,24325-44-8,29583-34-4,36779-79-0,60133-16-6,61277-90-5,61277-93-8
(1S,2S,4R)-2-norbornanol

Guidance literature:: With [RuCl₂(triphenylphosphine)₂(1,2-diaminoethane)]; potassium tert-butylate; hydrogen; In isopropyl alcohol; tert-butyl alcohol; at 20 ℃; under 7240.26 Torr; Reagent/catalyst; diastereoselective reaction; Inert atmosphere;
DOI:10.1021/op060063n

Reference yield: 93.0%

: 2-((1S,2S,4R)-Bicyclo[2.2.1]hept-2-yloxy)-tetrahydro-pyran

: 497-36-9,497-37-0,1632-68-4,24325-44-8,29583-34-4,36779-79-0,60133-16-6,61277-90-5,61277-93-8
(1S,2S,4R)-2-norbornanol

Guidance literature:: With trichloroisocyanuric acid; In methanol; at 20 ℃; for 4h;
DOI:10.1081/SCC-200031053

Reference yield: 92.0%

: 278-74-0
exo-2,3-epoxynorbornane

: 497-36-9,497-37-0,1632-68-4,24325-44-8,29583-34-4,36779-79-0,60133-16-6,61277-90-5,61277-93-8
(1S,2S,4R)-2-norbornanol

Guidance literature:: With N,N'-Dimethylurea; tris(pyrrolidino)phosphine oxide; lithium bromide; In tetrahydrofuran; at 20 ℃; Electrochemical reaction;
DOI:10.1126/science.aav5606