Vinpocetine Impurity L structure

Vinpocetine Impurity L

TL;DR: Vinpocetine Impurity L (CAS 58000-63-8) is a chemical compound with molecular formula C21H26N2O3 and molecular weight 354.19 g/mol, supplied by Kehong Biological (Henan Kehong Biological Technology Co., Ltd.) with CRO/CDMO custom synthesis services.

methyl (15S,17R,19R)-15-ethyl-17-hydroxy-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraene-17-carboxylate

Also Known As: vincamine, Vinpocetine Impurity L, Vinpocetine Impurity 11, (3R,14R,16S)-Vincamine, METHYL (41R,12R,13AS)-13A-ETHYL-12-HYDROXY-2,3,41,5,6,12,13,13A-OCTAHYDRO-1H-INDOLO[3,2,1-DE]PYRIDO[3,2,1-IJ][1,5]NAPHTHYRIDINE-12-CARBOXYLATE

CAS: 58000-63-8
Molecular Formula C21H26N2O3
Molecular Weight 354.19 g/mol
LogP 2.9525
Topological Polar Surface Area 54.7 Ų
Hydrogen Bond Donors 1
Hydrogen Bond Acceptors 4
Rotatable Bonds 2
Exact Mass 354.19434
Heavy Atoms 26
Complexity 904.0384

Chemical Identifiers

CAS Number 58000-63-8
SMILES CC[C@@]12CCCN3[C@H]1C4=C(CC3)C5=CC=CC=C5N4[C@@](C2)(C(=O)OC)O

Product Overview

Vinpocetine Impurity L (CAS 58000-63-8), with molecular formula C21H26N2O3 and molecular weight 354.19 g/mol. IUPAC: methyl (15S,17R,19R)-15-ethyl-17-hydroxy-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraene-17-carboxylate.

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Safety Data Sheet (MSDS / SDS) View the Laboratory Chemical Safety Summary (LCSS) on PubChem — includes GHS classifications, hazard statements, first aid measures, and handling precautions.
View MSDS →

Chemical Property Profile of Vinpocetine Impurity L

XLogP
2.9525
TPSA (Topological Polar Surface Area)
54.7
Hydrogen Bond Donors
1
Hydrogen Bond Acceptors
4
Rotatable Bonds
2
Heavy Atoms
26
Complexity
904.0384
Exact Mass
354.19434
Monoisotopic Mass
354.19434
Data Source: Chemical property values are referenced from PubChem, the world's largest open chemistry database maintained by the National Center for Biotechnology Information (NCBI), U.S. National Library of Medicine.

Property Insights of Vinpocetine Impurity L

The XLogP value of 2.9525 suggests moderate lipophilicity, balancing water solubility and membrane permeability for Vinpocetine Impurity L. With a topological polar surface area (TPSA) of 54.7 Ų, Vinpocetine Impurity L exhibits relatively low polarity, potentially indicating favorable cell membrane permeability. Following Lipinski's Rule of Five, Vinpocetine Impurity L has 1 hydrogen bond donor(s) and 4 hydrogen bond acceptor(s), all within the drug-like range, suggesting favorable oral bioavailability potential.

Frequently Asked Questions

What is the typical lead time for this product?
Lead time typically ranges from 3-7 business days for in-stock items. For larger quantities or custom orders, please contact us for specific lead times.
Can you provide samples for testing?
Yes, we offer sample quantities for quality testing. Please submit an inquiry with your requirements and we will arrange samples accordingly.
What documentation do you provide with the product?
We provide COA (Certificate of Analysis), MSDS (Material Safety Data Sheet), and technical data sheets with each shipment.
Do you ship internationally?
Yes, we ship to most countries worldwide. Shipping costs and delivery times vary by location. Please contact us for specific shipping information.

Frequently Asked Questions

What is the CAS number of Vinpocetine Impurity L?

The CAS number of Vinpocetine Impurity L is 58000-63-8.

What is the molecular formula of Vinpocetine Impurity L?

The molecular formula of Vinpocetine Impurity L is C21H26N2O3.

What is the molecular weight of Vinpocetine Impurity L?

The molecular weight of Vinpocetine Impurity L is 354.19 g/mol.

Where can I buy Vinpocetine Impurity L?

You can request a quote for Vinpocetine Impurity L directly from KEHONG BIO. Contact us or email info@kehongbio.com for pricing and availability.

Does KEHONG BIO offer custom synthesis for Vinpocetine Impurity L?

Yes, KEHONG BIO provides custom synthesis services for Vinpocetine Impurity L and related compounds. Contact us with your specific requirements including quantity, purity, and timeline.

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