5-[4-[3-chloro-4-[dideuterio-(3-fluorophenyl)methoxy]anilino]quinazolin-6-yl]furan-2-carbaldehyde


Chemical Name: 5-[4-[3-chloro-4-[dideuterio-(3-fluorophenyl)methoxy]anilino]quinazolin-6-yl]furan-2-carbaldehyde
CAS Number: 231278-84-5
Product Number: AG002M90(AGN-PC-0D1ZTN)
Synonyms:
MDL No:
Molecular Formula: C26H17ClFN3O3
Molecular Weight: 473.8829

Identification/Properties


Computed Properties
Molecular Weight:
473.888g/mol
XLogP3:
6.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
7
Exact Mass:
473.094g/mol
Monoisotopic Mass:
473.094g/mol
Topological Polar Surface Area:
77.2A^2
Heavy Atom Count:
34
Formal Charge:
0
Complexity:
675
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



5-(4-((3-Chloro-4-((3-fluorobenzyl)oxy)phenyl)amino)quinazolin-6-yl)furan-2-carbaldehyde is a versatile compound that plays a crucial role in chemical synthesis. This compound is commonly utilized as a key intermediate in the production of various pharmaceutical agents and organic compounds. Its unique structure and reactivity make it an indispensable building block in the synthesis of complex molecules.In chemical synthesis, this compound acts as a valuable starting material for the creation of novel drugs, agrochemicals, and materials. Its functional groups allow for selective modifications, enabling chemists to generate diverse derivatives with tailored properties. Additionally, the presence of heterocyclic rings provides opportunities for the development of biologically active compounds.Furthermore, the presence of a furan ring in the structure of 5-(4-((3-Chloro-4-((3-fluorobenzyl)oxy)phenyl)amino)quinazolin-6-yl)furan-2-carbaldehyde enhances its utility in the design of bioactive molecules. The furan ring contributes to the compound's aromaticity and can participate in various chemical reactions to introduce desired functionalities.Overall, the application of 5-(4-((3-Chloro-4-((3-fluorobenzyl)oxy)phenyl)amino)quinazolin-6-yl)furan-2-carbaldehyde in chemical synthesis is instrumental in the development of innovative compounds with diverse applications in the fields of medicine, agriculture, and materials science.