Ferutinine

Base Information

Chemical Name:Ferutinine
CAS No.:41743-44-6
Deprecated CAS:69500-35-2
Molecular Formula:C22H30O4
Molecular Weight:358.478
Hs Code.:
NSC Number:606959
DSSTox Substance ID:DTXSID20961947
Nikkaji Number:J917.648I
Wikidata:Q27452770
Pharos Ligand ID:33TCSQ3GC7FS
Metabolomics Workbench ID:136733
ChEMBL ID:CHEMBL465040
Mol file:41743-44-6.mol

Synonyms:4-oxy-6-(4-oxybezoyloxy)dauc-8,9-en;ferutinin;ferutinine

Suppliers and Price of Ferutinine

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

Sigma-Aldrich
Ferutinin ≥98% (HPLC)
5 mg
$ 113.00

Medical Isotopes, Inc.
Ferutinin
5 mg
$ 490.00

Cayman Chemical
Ferutinin ≥98%
5mg
$ 93.00

Cayman Chemical
Ferutinin ≥98%
1mg
$ 31.00

Cayman Chemical
Ferutinin ≥98%
10mg
$ 155.00

AK Scientific
Ferutinin
10mg
$ 309.00

Adipogen Life Sciences
Ferutinin(highpurity) ≥98%(HPLC)
5 mg
$ 95.00

Total 8 raw suppliers

Chemical Property of Ferutinine

Chemical Property:

Vapor Pressure:2.24E-10mmHg at 25°C
Boiling Point:489°C at 760 mmHg
Flash Point:164.4°C
PSA：66.76000
Density:1.16g/cm³
LogP:4.46110
XLogP3:4.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:358.21440943
Heavy Atom Count:26
Complexity:561

Purity/Quality:

97% ^*data from raw suppliers

Ferutinin ≥98% (HPLC) ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC=C(C=C3)O)(C(C)C)O)C
Isomeric SMILES:CC1=CC[C@]2(CC[C@]([C@@H]2[C@H](C1)OC(=O)C3=CC=C(C=C3)O)(C(C)C)O)C
Uses Ferutinin acts as an agonist for estrogen receptor (ER) α. It also increases calcium permeability of lipid bilayer membranes, mitochondria, thymocytes, sarcoplasmic reticulum, and liposomes.

Technology Process of Ferutinine

There total 5 articles about Ferutinine 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:

: 778584-24-0
3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3,3a,4,5,8,8a-octahydroazulen-4-yl 4-(pivaloyloxy)benzoate

: 41743-44-6,69500-35-2
ferutinin

Guidance literature:: With ethylenediamine; In dichloromethane; at 20 ℃; for 3h;
DOI:10.1111/cbdd.12670

Reference yield:

: 27914-73-4
4-acetoxybenzoyl chloride

: 41743-44-6,69500-35-2
ferutinin

Guidance literature:: Multi-step reaction with 2 steps

1: 50 percent / pyridine / 10 h / 35 - 40 °C

2: 0.05 g / K₂CO₃ / methanol / 2 h

With pyridine; potassium carbonate; In methanol;

Reference yield:

: 41690-67-9
1-isopropyl-3a,6-dimethyl-1,2,3,3a,4,7,8,8a-octahydroazulene-1,8-diol

: 41743-44-6,69500-35-2
ferutinin

Guidance literature:: Multi-step reaction with 2 steps

1: 50 percent / pyridine / 10 h / 35 - 40 °C

2: 0.05 g / K₂CO₃ / methanol / 2 h

With pyridine; potassium carbonate; In methanol;