2,2'-Bipyrimidine, 4,6-dichloro-5-(2-methoxyphenoxy)-


Chemical Name: 2,2'-Bipyrimidine, 4,6-dichloro-5-(2-methoxyphenoxy)-
CAS Number: 150728-13-5
Product Number: AG001MTM(AGN-PC-0CTCFB)
Synonyms:
MDL No:
Molecular Formula: C15H10Cl2N4O2
Molecular Weight: 349.1715

Identification/Properties


Computed Properties
Molecular Weight:
349.171g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
4
Exact Mass:
348.018g/mol
Monoisotopic Mass:
348.018g/mol
Topological Polar Surface Area:
70A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
361
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

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NMR Spectrum


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Chemical Structure



4,6-Dichloro-5-(2-methoxyphenoxy)-2,2-bipyrimidine is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. In organic synthesis, this compound serves as a valuable building block for the construction of various heterocyclic structures. Its 2,2-bipyrimidine core imparts rigidity and structural diversity, making it a key component in the design of functional molecules. One important application of 4,6-Dichloro-5-(2-methoxyphenoxy)-2,2-bipyrimidine is in the development of pharmaceutical intermediates. By incorporating this compound into synthetic pathways, chemists can access novel drug candidates with potential therapeutic properties. Furthermore, this compound is instrumental in the preparation of molecular probes and complex organic materials. Its chlorine and methoxy substituents enable selective functionalization, facilitating the creation of tailored compounds for specific applications.Overall, 4,6-Dichloro-5-(2-methoxyphenoxy)-2,2-bipyrimidine plays a crucial role in advancing chemical synthesis by providing a strategic building block with diverse synthetic possibilities.