(-)-EPIGLOBULOL

Base Information

Chemical Name:(-)-EPIGLOBULOL
CAS No.:88728-58-9
Molecular Formula:C15H26 O
Molecular Weight:222.3663
Hs Code.:
ChEMBL ID:CHEMBL2269082
Metabolomics Workbench ID:127657
Nikkaji Number:J498.771C
Wikidata:Q110184137
Mol file:88728-58-9.mol

Synonyms:1H-Cycloprop[e]azulen-4-ol,decahydro-1,1,4,7-tetramethyl-, [1aR-(1aa,4b,4aa,7a,7ab,7ba)]-; Epiglobulol (6CI);(-)-Epiglobulol; epi-Globulol

Suppliers and Price of (-)-EPIGLOBULOL

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

American Custom Chemicals Corporation
(-)-EPIGLOBULOL 95.00%
5MG
$ 505.40

Crysdot
Epiglobulol 95+%
5mg
$ 436.00

Total 11 raw suppliers

Chemical Property of (-)-EPIGLOBULOL

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Refractive Index:n20/D 1.496
Boiling Point:293.87°C at 760 mmHg
Flash Point:123.055°C
PSA：20.23000
Density:0.963g/cm³
LogP:3.46570
Storage Temp.:2-8°C
XLogP3:3.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:222.198365449
Heavy Atom Count:16
Complexity:309

Purity/Quality:

98%,99%, ^*data from raw suppliers

(-)-EPIGLOBULOL 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: 23-24/25

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:CC1CCC2C1C3C(C3(C)C)CCC2(C)O
Isomeric SMILES:C[C@@H]1CC[C@@H]2[C@@H]1[C@H]3[C@H](C3(C)C)CC[C@]2(C)O

Technology Process of (-)-EPIGLOBULOL

There total 3 articles about (-)-EPIGLOBULOL 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:

: 25246-27-9
alloaromadendrene

: 489-41-8,552-02-3,577-27-5,19078-39-8,51371-47-2,55659-76-2,64366-31-0,64665-36-7,77171-54-1,88728-58-9,133443-04-6,146864-34-8
ledol

: 489-41-8,552-02-3,577-27-5,19078-39-8,51371-47-2,55659-76-2,64366-31-0,64665-36-7,77171-54-1,88728-58-9,133443-04-6,146864-34-8
(+)-viridiflorol

Guidance literature:: With lithium aluminium tetrahydride; 3-chloro-benzenecarboperoxoic acid; Yield given. Multistep reaction. Yields of byproduct given; 1.) CHCl₃, RT, 30 min, 2.) Et₂O, RT, overnight;
DOI:10.1016/0040-4020(95)01079-3

Reference yield:

: 25246-27-9
alloaromadendrene

: 489-41-8,552-02-3,577-27-5,19078-39-8,51371-47-2,55659-76-2,64366-31-0,64665-36-7,77171-54-1,88728-58-9,133443-04-6,146864-34-8
ledol

: 489-41-8,552-02-3,577-27-5,19078-39-8,51371-47-2,55659-76-2,64366-31-0,64665-36-7,77171-54-1,88728-58-9,133443-04-6,146864-34-8
(+)-viridiflorol

Guidance literature:: With lithium aluminium tetrahydride; 3-chloro-benzenecarboperoxoic acid; Yield given. Multistep reaction. Yields of byproduct given; 1.) CHCl₃, RT, 30 min, 2.) Et₂O, RT, overnight;
DOI:10.1016/0040-4020(95)01079-3