2H-Pyrido[3,2-b]-1,4-oxazine, 3,4-dihydro-


Chemical Name: 2H-Pyrido[3,2-b]-1,4-oxazine, 3,4-dihydro-
CAS Number: 20348-23-6
Product Number: AG0028WO(AGN-PC-00LEER)
Synonyms:
MDL No: MFCD09025907
Molecular Formula: C7H8N2O
Molecular Weight: 136.1512

Identification/Properties


Properties
MP:
85 °C
BP:
285.7°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
136.154g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
136.064g/mol
Monoisotopic Mass:
136.064g/mol
Topological Polar Surface Area:
34.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
118
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


NMR Spectrum


Other Analytical Data


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Chemical Structure



The compound 3,4-Dihydro-2H-pyrido[3,2-b]-1,4-oxazine, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure and properties make it a valuable intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals. In chemical synthesis, $name$ is often used as a key starting material in the preparation of heterocyclic compounds with diverse structures and functionalities. Its reactivity allows for the introduction of different functional groups through various chemical transformations, enabling the synthesis of complex molecular structures efficiently.Furthermore, the presence of both nitrogen and oxygen atoms in its ring structure imparts specific reactivity patterns that are exploited in the development of new chemical entities. This structural motif is particularly valuable in the pharmaceutical industry, where the synthesis of heterocyclic compounds is a common strategy in drug discovery and development.Additionally, the ability of $name$ to undergo various types of chemical reactions, such as cyclization, substitution, and addition reactions, further expands its utility in chemical synthesis. This compound serves as a valuable tool for organic chemists seeking to design and prepare novel molecules with potential applications in the fields of medicine, agriculture, and materials science.