4-chloro-5-fluoroquinoline


Chemical Name: 4-chloro-5-fluoroquinoline
CAS Number: 1229037-03-9
Product Number: AG000JQT(AGN-PC-086DKP)
Synonyms:
MDL No:
Molecular Formula: C9H5ClFN
Molecular Weight: 181.5941

Identification/Properties


Computed Properties
Molecular Weight:
181.594g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
181.009g/mol
Monoisotopic Mass:
181.009g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
165
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-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



4-Chloro-5-fluoroquinoline is a versatile compound used in various chemical synthesis processes. This particular quinoline derivative serves as a valuable building block in the creation of pharmaceuticals, agrochemicals, and advanced materials. Its unique structure and properties make it an essential component in the development of novel compounds with diverse applications. In chemical synthesis, 4-Chloro-5-fluoroquinoline can be utilized as a key intermediate for the preparation of biologically active molecules and drug candidates. Its presence in the molecular structure imparts specific characteristics and functionalities that are crucial for pharmacological activity. By incorporating this compound into synthetic routes, chemists can control the reactivity, selectivity, and overall performance of the final products. Moreover, 4-Chloro-5-fluoroquinoline plays a vital role in the synthesis of specialty chemicals and materials. Its ability to undergo various reactions and transformations enables the creation of new compounds with tailored properties for specific industrial applications. Whether used as a catalyst, a ligand, or a molecular scaffold, this quinoline derivative offers diverse possibilities for chemical design and innovation. Overall, the application of 4-Chloro-5-fluoroquinoline in chemical synthesis extends far beyond its molecular structure. By leveraging its unique properties and reactivity, researchers and chemists can expedite the development of novel compounds with significant implications in pharmaceuticals, agrochemicals, and materials science.