1-Propanone,3-amino-1-(1-piperidinyl)-, hydrochloride (1:1)


Chemical Name: 1-Propanone,3-amino-1-(1-piperidinyl)-, hydrochloride (1:1)
CAS Number: 221043-84-1
Product Number: AG00BENP(AGN-PC-0QYQ18)
Synonyms:
MDL No:
Molecular Formula: C8H17ClN2O
Molecular Weight: 192.6864

Identification/Properties


Computed Properties
Molecular Weight:
192.687g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
192.103g/mol
Monoisotopic Mass:
192.103g/mol
Topological Polar Surface Area:
46.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
130
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:
2
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



3-Amino-1-(piperidin-1-yl)propan-1-one hydrochloride, also known as AP-221, is a versatile building block in chemical synthesis with a wide range of applications. This compound is commonly used in the pharmaceutical industry as a key intermediate in the synthesis of various drugs, particularly those targeting the central nervous system. In organic chemistry, 3-Amino-1-(piperidin-1-yl)propan-1-one hydrochloride serves as a valuable starting material for the preparation of complex molecules due to its unique structure and reactivity. It can undergo a variety of chemical transformations, including acylation, alkylation, and reductive amination, enabling the synthesis of diverse derivatives with tailored properties.Moreover, this compound plays a crucial role in the development of new materials, such as polymers and specialty chemicals, through its participation in multi-step synthesis pathways. Its presence in the chemical synthesis toolbox offers researchers and synthetic chemists the opportunity to explore innovative synthetic strategies and expand the scope of bioactive compounds and functional materials.