Ilicol

Base Information

Chemical Name:Ilicol
CAS No.:72715-02-7
Molecular Formula:C15H26O2
Molecular Weight:238.37
Hs Code.:
Mol file:72715-02-7.mol

Synonyms:ilicic alcohol;Gilvocacin V;gilvocarcin V;

Suppliers and Price of Ilicol

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

Crysdot
Ilicol 95+%
5mg
$ 860.00

Arctom
Ilicol ≥98%
5mg
$ 553.00

Total 21 raw suppliers

Chemical Property of Ilicol

Chemical Property:

Melting Point:134-135 °C
Boiling Point:350.9±25.0 °C(Predicted)
PKA:14.78±0.10(Predicted)
PSA：40.46000
Density:1.029±0.06 g/cm3(Predicted)
LogP:2.89240

Purity/Quality:

99% ^*data from raw suppliers

Ilicol 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Ilicol

There total 1 articles about Ilicol 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:

: 4586-68-9
4-hydroxy-11⁽¹³⁾-eudesmen-12-oic acid

: 72715-02-7
(1R,4aR,7R,8aR)-decahydro-7-(3-hydroxyprop-1-en-2-yl)-1,4a-dimethylnaphthalen-1-ol

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran;
DOI:10.1016/0031-9422(79)80148-X

Reference yield:

: 72715-02-7
(1R,4aR,7R,8aR)-decahydro-7-(3-hydroxyprop-1-en-2-yl)-1,4a-dimethylnaphthalen-1-ol

: 76497-23-9,88564-53-8,3650-40-6
costal

Guidance literature:: Multi-step reaction with 2 steps

1: 87 percent / Jones reagent

2: 56 percent / POCl₃; pyridine / -20 °C

With pyridine; jones reagent; trichlorophosphate;
DOI:10.1016/j.bmcl.2005.05.053