5-[4-((3-Chloro-4-((3-fluorobenzyl)oxy)phenyl)amino)quinazolin-6-yl]-2-furaldehyde丨CAS 231278-84-5

5-[4-((3-Chloro-4-((3-fluorobenzyl)oxy)phenyl)amino)quinazolin-6-yl]-2-furaldehyde丨CAS 231278-84-5
Product Introduction:
Catalog No.: SS141243
CAS No.: 231278-84-5
Assay: 98.0%~102.0% (Calculated on the dried basis)
Product Name: 5-[4-((3-Chloro-4-((3-fluorobenzyl)oxy)phenyl)amino)quinazolin-6-yl]-2-furaldehyde
Molecular Formula: C26H17ClFN3O3
Molecular Weight: 473.88
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Technical Parameters
Description

Hangzhou Leap Chem Co., Ltd. is one of the most professional manufacturers and suppliers of 5-[4-((3-chloro-4-((3-fluorobenzyl)oxy)phenyl)amino)quinazolin-6-yl]-2-furaldehyde丨cas 231278-84-5 in China. Welcome to wholesale bulk high quality chemical products at competitive price from our factory. If you have any enquiry about custom service, please feel free to email us.

 

Specifications

 

Appearance Yellow to greenish yellow colored powder
Assay 98.0% ~ 102.0% (Calculated on the dried basis)
Solubility Slightly soluble in dimethylformamide
Identification HPLC: The retention time of the major peak in the chromatogram of the sample solution must correspond to that of the standard solution as obtained in the related substances
Loss on drying 5.0% max
Residue on ignition 0.5% max
Related Substance - Impurity A 0.15% max
Related Substance - Impurity B 0.10% max
Related Substance - Impurity C 0.10% max
Related Substance - Impurity D 0.10% max
Related Substance - Impurity E 0.10% max
Related Substance - Impurity F 0.10% max
Related Substance - Impurity G 0.10% max
Related Substance - Impurity H 0.05% max
Any other individual impurity 0.5% max
Total impurities 1.0% max

 

 

 

Applications

 

5-[4-((3-Chloro-4-((3-fluorobenzyl)oxy)phenyl)amino)quinazolin-6-yl]-2-furaldehyde is a highly functionalized small molecule primarily used in pharmaceutical research and medicinal chemistry. It serves as a key intermediate in the development of kinase inhibitors and other targeted therapeutic compounds, where the quinazoline core provides a scaffold for receptor and enzyme interaction. The molecule is applied in structure–activity relationship (SAR) studies to optimize potency, selectivity, and pharmacokinetic properties of drug candidates. Its furaldehyde and substituted phenyl groups allow further chemical modifications, enabling exploration of diverse derivatives in drug discovery programs. In addition, this compound is used in preclinical research for enzyme inhibition assays, receptor binding studies, and mechanistic investigations of signal transduction pathways relevant to cancer and other proliferative diseases.

 

Benefits

 

The benefits of this compound arise from its multifunctional structure, synthetic versatility, and suitability for precision medicinal chemistry. The quinazoline core provides strong receptor-binding potential, while the chloro, fluoro, and furan aldehyde substituents allow targeted chemical modifications to enhance bioactivity and selectivity. Its well-defined molecular structure supports reproducible synthesis, high-purity isolation, and reliable incorporation into multi-step synthetic pathways. The molecule's functional groups enable diverse reactions, including condensation, nucleophilic substitution, and coupling, facilitating rapid analog generation for SAR optimization. Its compatibility with standard organic solvents and laboratory conditions ensures ease of handling in research and development settings.

 

Conclusion

 

5-[4-((3-Chloro-4-((3-fluorobenzyl)oxy)phenyl)amino)quinazolin-6-yl]-2-furaldehyde is a versatile and valuable intermediate in pharmaceutical and medicinal chemistry research. Its multifunctional structure and chemical reactivity enable the design and synthesis of targeted drug candidates, particularly kinase inhibitors and receptor-modulating compounds. By supporting efficient derivative generation, SAR exploration, and preclinical studies, this compound remains an essential tool in modern drug discovery and chemical biology applications.

 

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