Erlotinib Impurity 14 structure

Erlotinib Impurity 14

TL;DR: Erlotinib Impurity 14 (CAS 299912-60-0) is a chemical compound with molecular formula C25H29N3O5 and molecular weight 451.21 g/mol, supplied by Kehong Biological (Henan Kehong Biological Technology Co., Ltd.) with CRO/CDMO custom synthesis services.

4-[3-[[6,7-bis(2-methoxyethoxy)quinazolin-4-yl]amino]phenyl]-2-methylbut-3-yn-2-ol

Also Known As: Erlotinib Impurity 14, Erlotinib Impurity 77, 4-(3-((6,7-bis(2-methoxyethoxy)quinazolin-4-yl)amino)phenyl)-2-methylbut-3-yn-2-ol, 4-[3-[[6,7-bis(2-methoxyethoxy)-4-quinazolinyl]amino]phenyl]-2-methyl-3-butyn-2-ol, 4-[3-[[6,7-bis(2-methoxyethoxy)quinazolin-4-yl]amino]phenyl]-2-methyl-but-3-yn-2-ol

CAS: 299912-60-0
Molecular Formula C25H29N3O5
Molecular Weight 451.21 g/mol
LogP 3.5462
Topological Polar Surface Area 94.96 Ų
Hydrogen Bond Donors 2
Hydrogen Bond Acceptors 8
Rotatable Bonds 10
Exact Mass 451.21072
Heavy Atoms 33
Complexity 1132.3162

Chemical Identifiers

CAS Number 299912-60-0
SMILES CC(C)(C#CC1=CC(=CC=C1)NC2=NC=NC3=CC(=C(C=C32)OCCOC)OCCOC)O

Product Overview

Erlotinib Impurity 14 (CAS 299912-60-0), with molecular formula C25H29N3O5 and molecular weight 451.21 g/mol. IUPAC: 4-[3-[[6,7-bis(2-methoxyethoxy)quinazolin-4-yl]amino]phenyl]-2-methylbut-3-yn-2-ol.

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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 Erlotinib Impurity 14

XLogP
3.5462
TPSA (Topological Polar Surface Area)
94.96
Hydrogen Bond Donors
2
Hydrogen Bond Acceptors
8
Rotatable Bonds
10
Heavy Atoms
33
Complexity
1132.3162
Exact Mass
451.21072
Monoisotopic Mass
451.21072
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 Erlotinib Impurity 14

The XLogP value of 3.5462 indicates that Erlotinib Impurity 14 is lipophilic (fat-soluble), which may influence its absorption, distribution, and formulation strategy. The TPSA of 94.96 Ų falls within the moderate polarity range, balancing permeability and solubility for Erlotinib Impurity 14. Following Lipinski's Rule of Five, Erlotinib Impurity 14 has 2 hydrogen bond donor(s) and 8 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 Erlotinib Impurity 14?

The CAS number of Erlotinib Impurity 14 is 299912-60-0.

What is the molecular formula of Erlotinib Impurity 14?

The molecular formula of Erlotinib Impurity 14 is C25H29N3O5.

What is the molecular weight of Erlotinib Impurity 14?

The molecular weight of Erlotinib Impurity 14 is 451.21 g/mol.

Where can I buy Erlotinib Impurity 14?

You can request a quote for Erlotinib Impurity 14 directly from KEHONG BIO. Contact us or email info@kehongbio.com for pricing and availability.

Does KEHONG BIO offer custom synthesis for Erlotinib Impurity 14?

Yes, KEHONG BIO provides custom synthesis services for Erlotinib Impurity 14 and related compounds. Contact us with your specific requirements including quantity, purity, and timeline.

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