Venoterpine

Base Information

• Chemical Name: Venoterpine
• CAS No.: 17948-42-4
• Molecular Formula: C9H11NO
• Molecular Weight: 149.19
• Nikkaji Number: J2.364.925J
• Wikidata: Q105116682
• Metabolomics Workbench ID: 44233
• Mol file: 17948-42-4.mol

Synonyms:Venoterpine;7-methyl-6,7-dihydro-5H-cyclopenta[c]pyridin-6-ol;17948-42-4;Gentialutine;Isogentialutine;Alkaloid RW47;CHEBI:172412;7-methyl-5H,6H,7H-cyclopenta[c]pyridin-6-ol

Chemical Property of Venoterpine

Chemical Property:

• Melting Point: 128-130°C
• PSA: 33.12000
• LogP: 1.10210
• XLogP3: 0.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 149.084063974
• Heavy Atom Count: 11
• Complexity: 149

Purity/Quality:

HPLC≥98% ^*data from raw suppliers

Venoterpine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1C(CC2=C1C=NC=C2)O
• Description: This monoterpenoid alkaloid occurs in Alstonia venenata, being present in the fruit to the extent of 0.0008 per cent. The earlier structure based upon the infra_x0002_red and NMR spectra has recently been modified to that given above, determined from ORO-CD data and comparison with L-( - )-Actinidine.

Technology Process of Venoterpine

There total 1 articles about Venoterpine 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:

(6S,7R)-6-Hydroxy-7-methyl-6,7-dihydro-5H-[2]pyrindine-4-carboxylic acid → venoterpine (17948-42-4,55399-77-4,55399-78-5)

Guidance literature:

vacuum flash pyrolysis;

DOI:10.1016/S0040-4039(00)61942-1

Refernces