trans-beta-Santalol

Base Information

Chemical Name:trans-beta-Santalol
CAS No.:37172-32-0
Molecular Formula:C15H24 O
Molecular Weight:220.355
Hs Code.:
DSSTox Substance ID:DTXSID10885663
Nikkaji Number:J422.364K
Wikidata:Q67880221
Metabolomics Workbench ID:47466
Mol file:37172-32-0.mol

Synonyms:trans-beta-Santalol;37172-32-0;(e)-beta-santalol;2-Penten-1-ol, 2-methyl-5-((1S,2R,4R)-2-methyl-3-methylenebicyclo(2.2.1)hept-2-yl)-, (2E)-;2-Penten-1-ol, 2-methyl-5-[(1S,2R,4R)-2-methyl-3-methylenebicyclo[2.2.1]hept-2-yl]-, (2E)-;ss-Santalol;trans-b-Santalol;beta-trans-Santalol;(-)-trans-beta-Santalol;(-)-(E)-beta-Santalol;SCHEMBL654806;SCHEMBL6512180;DTXSID10885663;Q67880221;(2E)-2-methyl-5-[(1S,2R,4R)-2-methyl-3-methylidenebicyclo[2.2.1]heptan-2-yl]pent-2-en-1-ol;(E)-2-Methyl-5-[(1S,4R)-2-methyl-3-methylenebicyclo[2.2.1]heptane-2beta-yl]-2-pentene-1-ol;2-Penten-1-ol, 2-methyl-5-(2-methyl-3-methylenebicyclo[2.2.1]hept-2-yl)-, [1S-[1.alpha.,2.alpha.(E),4.alpha.]]-

Suppliers and Price of trans-beta-Santalol

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 4 raw suppliers

Chemical Property of trans-beta-Santalol

Chemical Property:

Vapor Pressure:4.81E-05mmHg at 25°C
Boiling Point:312°C at 760 mmHg
Flash Point:116.3°C
PSA：20.23000
Density:0.97g/cm³
LogP:3.69760
XLogP3:4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:220.182715385
Heavy Atom Count:16
Complexity:315

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=CCCC1(C2CCC(C2)C1=C)C)CO
Isomeric SMILES:C/C(=C\CC[C@@]1([C@H]2CC[C@H](C2)C1=C)C)/CO

Technology Process of trans-beta-Santalol

There total 27 articles about trans-beta-Santalol 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:

: 77-42-9,27542-07-0,27542-08-1,37172-32-0,42495-69-2,73890-74-1,77983-61-0,79081-89-3,79081-90-6,81893-42-7,98718-53-7,98718-54-8,130930-05-1,131726-06-2,131726-07-3
santalol

Guidance literature:: X, Lithiumaluminiumhydrid;
DOI:10.1016/S0040-4039(01)87560-2

Reference yield:

: 81967-89-7
β-santalene

: 77-42-9,27542-07-0,27542-08-1,37172-32-0,42495-69-2,73890-74-1,77983-61-0,79081-89-3,79081-90-6,81893-42-7,98718-53-7,98718-54-8,130930-05-1,131726-06-2,131726-07-3
rac-(Z)-β-santalol

Guidance literature:: β-santalene; With selenium(IV) oxide; In ethanol; for 4h; Heating;

With sodium tetrahydroborate; at 20 ℃;
DOI:10.1055/s-2005-864825

Reference yield:

: Dimethyl-[3-methyl-3-(4-methyl-pent-3-enyl)-bicyclo[2.2.1]hept-(2Z)-ylidenemethyl]-phenyl-silane

: 77-42-9,27542-07-0,27542-08-1,37172-32-0,42495-69-2,73890-74-1,77983-61-0,79081-89-3,79081-90-6,81893-42-7,98718-53-7,98718-54-8,130930-05-1,131726-06-2,131726-07-3
rac-(Z)-β-santalol

Guidance literature:: Multi-step reaction with 2 steps

1.1: 100 percent / HI / 5 h / Heating

2.1: SeO₂ / ethanol / 4 h / Heating

2.2: 68 mg / NaBH₄ / 20 °C

With selenium(IV) oxide; hydrogen iodide; In ethanol;
DOI:10.1055/s-2005-864825