3-oxa-9-azabicyclo[3.3.1]nonan-7-one;hydrochloride


Chemical Name: 3-oxa-9-azabicyclo[3.3.1]nonan-7-one;hydrochloride
CAS Number: 1126795-00-3
Product Number: AG003JUK(AGN-PC-0NUVSM)
Synonyms:
MDL No: MFCD20491410
Molecular Formula: C7H12ClNO2
Molecular Weight: 177.6287

Identification/Properties


Properties
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
177.628g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
177.056g/mol
Monoisotopic Mass:
177.056g/mol
Topological Polar Surface Area:
38.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
144
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information


NMR Spectrum


Other Analytical Data


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Chemical Structure



3-Oxa-9-azabicyclo[3.3.1]nonan-7-one, hydrochloride (1:1) is a versatile compound used in chemical synthesis for its unique properties. Its structural composition allows it to serve as a key building block in the creation of various complex molecules, making it invaluable in the field of organic chemistry.This compound is particularly useful in the synthesis of heterocyclic compounds and pharmaceutical intermediates. Its presence in a reaction mixture can facilitate the formation of new carbon-carbon and carbon-nitrogen bonds, leading to the creation of novel compounds with potential applications in drug discovery and development.Additionally, 3-Oxa-9-azabicyclo[3.3.1]nonan-7-one, hydrochloride (1:1) can act as a catalyst or a ligand in certain chemical transformations, enhancing the efficiency and selectivity of reactions. Its ability to participate in various chemical processes makes it a valuable tool for chemists seeking to synthesize complex molecules with specific structures and properties.Overall, the application of 3-Oxa-9-azabicyclo[3.3.1]nonan-7-one, hydrochloride (1:1) in chemical synthesis enables researchers to explore new avenues in organic chemistry, leading to the development of innovative compounds with potential industrial and medicinal significance.