Isorauhimbinic acid

Base Information

Chemical Name:Isorauhimbinic acid
CAS No.:483-05-6
Molecular Formula:C₂₀H₂₄N₂O₃
Molecular Weight:340.422
Hs Code.:
ChEMBL ID:CHEMBL465592
DSSTox Substance ID:DTXSID901209228
Metabolomics Workbench ID:136865
Nikkaji Number:J2.200.529D

Synonyms:Isorauhimbinic acid;CHEMBL465592;DTXSID901209228;BDBM50269441;483-05-6;(3beta,16beta,17alpha,20alpha)-17-Hydroxyyohimban-16-carboxylic acid

Suppliers and Price of Isorauhimbinic acid

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
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price

Total 0 raw suppliers

Chemical Property of Isorauhimbinic acid

Chemical Property:

XLogP3:0.3
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:340.17869263
Heavy Atom Count:25
Complexity:541

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CC(C(C2C1CN3CCC4=C(C3C2)NC5=CC=CC=C45)C(=O)O)O
Isomeric SMILES:C1C[C@@H]([C@H]([C@@H]2[C@H]1CN3CCC4=C([C@H]3C2)NC5=CC=CC=C45)C(=O)O)O

Technology Process of Isorauhimbinic acid

There total 2 articles about Isorauhimbinic acid 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:

: 483-05-6,522-85-0,522-86-1,522-87-2,572-69-0
17α-hydroxy-20α-yohimban-16α-carboxylic acid

Guidance literature:: With potassium hydroxide;

Reference yield:

: 483-05-6,522-85-0,522-86-1,522-87-2,572-69-0
17α-hydroxy-20α-yohimban-16α-carboxylic acid

Guidance literature:: Aus der technischen Endlauge der Yohimbingewinnung durch fraktionierte Faellung mit Ammoniak und Trennung von Yohimbinsaeure ueber die Hydrochloride oder durch Fraktionierung aus Methanol oder Alkohol;