Yohimbic acid, ethyl ester

Base Information

• Chemical Name: Yohimbic acid, ethyl ester
• CAS No.: 73840-32-1
• Molecular Formula: C₂₂H₂₈N₂O₃
• Molecular Weight: 368.476
• DSSTox Substance ID: DTXSID00994970
• Nikkaji Number: J107.290K
• Wikidata: Q76155530
• Mol file: 73840-32-1.mol

Synonyms:Yohimbic acid, ethyl ester;73840-32-1;Yohimbosaeureaethylester;Yohimbosaeureaethylester [German];BRN 6119015;A 38;2-25-00-00212 (Beilstein Handbook Reference);Yohimban-16-alpha-carboxylic acid, 17-alpha-hydroxy-, ethyl ester;DTXSID00994970;AKOS040749824;Ethyl 17-hydroxyyohimban-16-carboxylate;ethyl (1S,15R,18S,19R,20S)-18-hydroxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate;LS-162733;Yohimban-16-carboxylic acid, 17-hydroxy-, ethyl ester, (16.alpha.,17.alpha.)-;ethyl (1R,2S,4aR,13bS,14aS)-2-hydroxy-1,2,3,4,4a,5,7,8,13,13b,14,14a-dodecahydroindolo[2',3':3,4]pyrido[1,2-b]isoquinoline-1-carboxylate

Chemical Property of Yohimbic acid, ethyl ester

Chemical Property:

• Vapor Pressure: 5.19E-13mmHg at 25°C
• Boiling Point: 551.8°C at 760 mmHg
• Flash Point: 287.5°C
• PSA: 65.56000
• Density: 1.29g/cm³
• LogP: 2.97510
• XLogP3: 3.3
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 368.20999276
• Heavy Atom Count: 27
• Complexity: 570

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCOC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O
• Isomeric SMILES: CCOC(=O)[C@H]1[C@H](CC[C@@H]2[C@@H]1C[C@H]3C4=C(CCN3C2)C5=CC=CC=C5N4)O

Technology Process of Yohimbic acid, ethyl ester

There total 8 articles about Yohimbic acid, ethyl ester 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:

→ 17α-hydroxy-20α-yohimban-16β-carboxylic acid ethyl ester (73840-32-1)

Guidance literature:

With hydrogenchloride;

Reference yield:

→ 17α-hydroxy-yohimban-16β-carboxylic acid ethyl ester (73840-32-1)

Guidance literature:

With hydrogenchloride;

Reference yield:

→ 17β-hydroxy-yohimban-16α-carboxylic acid ethyl ester (73840-32-1)

Guidance literature:

With hydrogenchloride;

upstream raw materials:

ethanol

yohimbinic acid

corynanthine