FERULENOL

Base Information

Chemical Name:FERULENOL
CAS No.:6805-34-1
Molecular Formula:C₂₄H₃₀O₃
Molecular Weight:366.5
Hs Code.:2932209090
Mol file:6805-34-1.mol

Synonyms:2H-1-Benzopyran-2-one,4-hydroxy-3-(3,7,11-trimethyl-2,6,10-dodecatrienyl)-, (E,E)-;2H-1-Benzopyran-2-one,4-hydroxy-3-[(2E,6E)-3,7,11-trimethyl-2,6,10-dodecatrienyl]- (9CI); Coumarin,4-hydroxy-3-(3,7,11-trimethyl-2,6,10-dodecatrienyl)- (7CI,8CI); Ferulenol

Suppliers and Price of FERULENOL

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

Usbiological
Ferulenol
1mg
$ 282.00

TRC
Ferulenol
1mg
$ 45.00

Cayman Chemical
Ferulenol ≥95%
1mg
$ 35.00

Cayman Chemical
Ferulenol ≥95%
10mg
$ 243.00

Cayman Chemical
Ferulenol ≥95%
5mg
$ 139.00

ApexBio Technology
Ferulenol
10mg
$ 300.00

ApexBio Technology
Ferulenol
5mg
$ 172.00

American Custom Chemicals Corporation
FERULENOL 95.00%
1MG
$ 169.05

American Custom Chemicals Corporation
FERULENOL 95.00%
5MG
$ 505.51

AK Scientific
Ferulenol
10mg
$ 402.00

Total 6 raw suppliers

Chemical Property of FERULENOL

Chemical Property:

Vapor Pressure:1.57E-10mmHg at 25°C
Melting Point:55-56℃
Boiling Point:492.8°C at 760 mmHg
PKA:4.50±1.00(Predicted)
Flash Point:161.7°C
PSA：50.44000
Density:1.07g/cm³
LogP:6.46030
Solubility.:Soluble in DMSO

Purity/Quality:

98% ^*data from raw suppliers

Ferulenol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses Ferulenol is antibiotic useful against mycobacteria similar to taxol.

Technology Process of FERULENOL

There total 5 articles about FERULENOL 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: 10.0%

: 6784-45-8,67023-85-2,72132-86-6,67023-84-1
(2E,6E)-farnesyl chloride

: 13546-81-1
sodium salt of 4-hydroxy coumarin

: 6805-34-1
E,E-3-farnesyl-4-hydroxycoumarin

Guidance literature:: In water; at 100 ℃; for 2.5h;
DOI:10.1016/j.bmc.2007.01.014

Reference yield: 4.0%

: 1076-38-6,92395-12-5
4-hydroxy[1]benzopyran-2-one

: 6805-34-1
E,E-3-farnesyl-4-hydroxycoumarin

Guidance literature:: With sodium hydroxide; for 3h; sonication;

Reference yield:

: 106-28-5
Farnesol

: 6805-34-1
E,E-3-farnesyl-4-hydroxycoumarin

Guidance literature:: Multi-step reaction with 2 steps

1: 97 percent / phosphorous trichloride / diethyl ether / 1.75 h / -5 - 20 °C

2: 10 percent / H₂O / 2.5 h / 100 °C

With phosphorus trichloride; In diethyl ether; water;
DOI:10.1016/j.bmc.2007.01.014