Virodhamine

Base Information

Chemical Name:Virodhamine
CAS No.:287937-12-6
Molecular Formula:C₂₂H₃₇NO₂
Molecular Weight:347.541
Hs Code.:
DSSTox Substance ID:DTXSID601018179
Nikkaji Number:J2.296.725H
Wikipedia:Virodhamine
Wikidata:Q4463
Pharos Ligand ID:6QPQ63CTL254
Metabolomics Workbench ID:10
ChEMBL ID:CHEMBL187349
Mol file:287937-12-6.mol

Synonyms:O-arachidonoyl ethanolamine;O-arachidonyl ethanol amine;virodhamine

Suppliers and Price of Virodhamine

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

TRC
Virodhamine
10mg
$ 130.00

American Custom Chemicals Corporation
VIRODHAMINE 95.00%
5MG
$ 290.40

Total 6 raw suppliers

Chemical Property of Virodhamine

Chemical Property:

Boiling Point:450.3±45.0 °C(Predicted)
PKA:7.68±0.10(Predicted)
PSA：52.32000
Density:0.930±0.06 g/cm3(Predicted)
LogP:6.33430
Storage Temp.:Desiccate at -20°C
XLogP3:5.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:17
Exact Mass:347.282429423
Heavy Atom Count:25
Complexity:408

Purity/Quality:

99% ^*data from raw suppliers

Virodhamine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCC=CCC=CCC=CCC=CCCCC(=O)OCCN
Isomeric SMILES:CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OCCN
Uses Virodhamine is an endogenous cannabinoid receptor mixed antagonist/agonist.

Technology Process of Virodhamine

There total 2 articles about Virodhamine 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: 73.0%

: 506-32-1,236743-58-1
all cis 5,8,11,14-eicosatetraenoic acid

: 26690-80-2
2-(N-tert-butoxycarbonylamino)ethanol

: 287937-12-6
virodhamine

Guidance literature:: all cis 5,8,11,14-eicosatetraenoic acid; With pyridine; In acetonitrile; at 0 - 4 ℃; for 1.5h; Irradiation;

2-(N-tert-butoxycarbonylamino)ethanol; With dmap; In acetonitrile; for 1.5h; Inert atmosphere;

With trifluoroacetic acid; In dichloromethane;
DOI:10.3390/ijms22020622