4,7-dichloro-1,6-naphthyridine


Chemical Name: 4,7-dichloro-1,6-naphthyridine
CAS Number: 952138-13-5
Product Number: AG00IITX(AGN-PC-0ALRWU)
Synonyms:
MDL No:
Molecular Formula: C8H4Cl2N2
Molecular Weight: 199.0368

Identification/Properties


Computed Properties
Molecular Weight:
199.034g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
197.975g/mol
Monoisotopic Mass:
197.975g/mol
Topological Polar Surface Area:
25.8A^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



4,7-Dichloro-1,6-naphthyridine is a versatile building block widely employed in chemical synthesis. This compound serves as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and materials. Its unique structure and reactivity make it an essential tool for chemists in the creation of novel molecules with diverse applications.In organic synthesis, 4,7-Dichloro-1,6-naphthyridine is commonly used to introduce specific functionalities or structural motifs into target compounds. Its ability to undergo various chemical transformations, such as substitution, addition, and cyclization reactions, enables the efficient construction of complex molecular frameworks. This compound plays a crucial role in the synthesis of heterocyclic compounds and derivatives, which are prevalent in drug discovery and material science.Furthermore, the distinct properties of 4,7-Dichloro-1,6-naphthyridine make it a valuable component in the design of bioactive molecules. By strategically incorporating this building block into molecular structures, chemists can modulate the properties and biological activities of the final compounds. This versatility makes 4,7-Dichloro-1,6-naphthyridine an indispensable tool for medicinal chemistry, offering opportunities for the development of new therapies and agrochemicals.Overall, the strategic use of 4,7-Dichloro-1,6-naphthyridine in chemical synthesis enables researchers to access a wide range of structurally diverse compounds with tailored properties. Its significance in modern organic chemistry lies in its ability to facilitate the efficient construction of complex molecules and the discovery of new materials and pharmaceuticals.