Vincamine

Base Information

Chemical Name:Vincamine
CAS No.:1617-90-9
Molecular Formula:C21H26N2O3
Molecular Weight:354.449
Hs Code.:29399990
European Community (EC) Number:216-576-3
UNII:996XVD0JHT
DSSTox Substance ID:DTXSID9040134
Nikkaji Number:J7.533G
Wikipedia:Vincamine
Wikidata:Q416225
NCI Thesaurus Code:C87697
Pharos Ligand ID:DD44FJKHMUUY
Metabolomics Workbench ID:53514
ChEMBL ID:CHEMBL1165342
Mol file:1617-90-9.mol

Synonyms:Cerebroxine;Devincan;Pervincamine;Vincamine;Vincapront;Vincimax

Suppliers and Price of Vincamine

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
Vincamine
20mg
$ 320.00

TRC
Vincamine
2.5g
$ 110.00

TCI Chemical
Vincamine >98.0%(T)
5g
$ 257.00

TCI Chemical
Vincamine >98.0%(T)
1g
$ 77.00

Sigma-Aldrich
Vincamine 98%
1g
$ 98.00

Sigma-Aldrich
Vincamine analytical standard
50mg
$ 95.00

Medical Isotopes, Inc.
Vincamine
25 mg
$ 1500.00

Crysdot
Vincamine 98+%
25g
$ 375.00

ChemScene
Vincamine 99.76%
500mg
$ 108.00

ChemScene
Vincamine 99.76%
100mg
$ 60.00

Total 181 raw suppliers

Chemical Property of Vincamine

Chemical Property:

Appearance/Colour:white to almost white fine crystalline powder
Vapor Pressure:0mmHg at 25°C
Melting Point:232 °C (dec.)(lit.)
Refractive Index:1.6500 (estimate)
Boiling Point:508.9 °C at 760 mmHg
PKA:12.13±0.40(Predicted)
Flash Point:261.6 °C
PSA：54.70000
Density:1.36 g/cm³
LogP:2.89040
Storage Temp.:2-8°C
Solubility.:Chloroform (Slightly), DMSO (Slightly)
XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:354.19434270
Heavy Atom Count:26
Complexity:598

Purity/Quality:

99.89% ^*data from raw suppliers

Vincamine ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xn
Hazard Codes:Xn
Statements: 22
Safety Statements: 36-26

MSDS Files:

Useful:

Canonical SMILES:CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)(C(=O)OC)O
Isomeric SMILES:CC[C@@]12CCCN3[C@@H]1C4=C(CC3)C5=CC=CC=C5N4[C@](C2)(C(=O)OC)O
Uses Vincamine is often used as a nootropic agent to combat the effects of aging, or in conjunction with other nootropics (such as piracetam) for a variety of purposes. Vincamine is a peripheral vasodilator that increases blood flow to the brain. vasodilator
Therapeutic Function Vasodilator

Technology Process of Vincamine

There total 96 articles about Vincamine 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: 84.7%

: 142892-63-5
(+)-15α-Chloro-vincamine

: 1617-90-9
vincamin

Guidance literature:: With hydrogen; potassium carbonate; triethylamine; palladium on activated charcoal; In methanol; for 6h; Ambient temperature;
DOI:10.1016/S0040-4020(01)81593-3

Reference yield: 78.3%

: 3247-10-7
(-)-vincadifformine

: 1617-90-9
vincamin

Guidance literature:: (-)-vincadifformine; With monoperoxymaleic acid; In methanol; at -5 - 0 ℃; for 6.16667h;

With sodium dithionate; at 40 ℃; for 3h; Reagent/catalyst;