longiborneol

Base Information

Chemical Name:longiborneol
CAS No.:465-24-7
Deprecated CAS:11075-64-2,29642-46-4
Molecular Formula:C15H26 O
Molecular Weight:222.371
Hs Code.:
DSSTox Substance ID:DTXSID20911841
Wikidata:Q82882050
Mol file:465-24-7.mol

Synonyms:1,4-Methanoazulen-9-ol,decahydro-1,5,5,8a-tetramethyl-, (1R,3aR,4S,8aS,9S)-(+)- (8CI);1,4-Methanoazulen-9-ol, decahydro-1,5,5,8a-tetramethyl-, [1R-(1a,3ab,4a,8ab,9S*)]-; Juniperol (6CI,7CI);(+)-Juniperol; (+)-Longiborneol; Longiborneol; Macrocarpol

Suppliers and Price of longiborneol

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 9 raw suppliers

Chemical Property of longiborneol

Chemical Property:

Melting Point:112°C
Refractive Index:1.5190 (estimate)
Boiling Point:303.56°C (rough estimate)
PKA:14.99±0.70(Predicted)
PSA：20.23000
Density:1.0441
LogP:3.60980
XLogP3:4.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:222.198365449
Heavy Atom Count:16
Complexity:321

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1(CCCC2(C3C1C(C2(CC3)C)O)C)C
Isomeric SMILES:CC1(CCCC2(C3C1[C@@H](C2(CC3)C)O)C)C

Technology Process of longiborneol

There total 11 articles about longiborneol 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%

: 119018-52-9
C₁₅H₂₄O

: 465-24-7
1,4-methanoazulen-9-ol, decahydro-1,5,5,8α-tetramethyl-(1R,3αR,4S,8αS,9S)-

Guidance literature:: With hydrogen; platinum(IV) oxide; In acetic acid; for 12h; under 2052 Torr; Ambient temperature;

Reference yield: 92.0%

: 465-26-9
8-oxolongibornane

: 465-24-7,16846-28-9,18374-92-0,27551-75-3,51897-51-9
(+)-isolongiborneol

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 3h;

Reference yield:

: 465-24-7
1,4-methanoazulen-9-ol, decahydro-1,5,5,8α-tetramethyl-(1R,3αR,4S,8αS,9S)-

: 465-24-7,16846-28-9,18374-92-0,27551-75-3,51897-51-9
(+)-isolongiborneol

Guidance literature:: Multi-step reaction with 2 steps

1: PCC / CH₂Cl₂

2: LiAlH₄ / tetrahydrofuran

With lithium aluminium tetrahydride; pyridinium chlorochromate; In tetrahydrofuran; dichloromethane;
DOI:10.1039/c39860001691