Benzamide, 4-amino-N-[2-(diethylamino)ethyl]-, monohydrochloride


Chemical Name: Benzamide, 4-amino-N-[2-(diethylamino)ethyl]-, monohydrochloride
CAS Number: 614-39-1
Product Number: AG00IAUY(AGN-PC-0T0GIN)
Synonyms:
MDL No:
Molecular Formula: C13H22ClN3O
Molecular Weight: 271.7863

Identification/Properties


Computed Properties
Molecular Weight:
271.789g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
6
Exact Mass:
271.145g/mol
Monoisotopic Mass:
271.145g/mol
Topological Polar Surface Area:
58.4A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
221
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

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NMR Spectrum


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Chemical Structure



4-Amino-N-[2-(diethylamino)ethyl]benzamide monohydrochloride is a versatile compound widely utilized in chemical synthesis processes. This compound serves as a crucial building block for the creation of various pharmaceuticals, agrochemicals, and fine chemicals due to its unique chemical properties. In organic synthesis, it can be used as a key intermediate in the development of novel and potent drug candidates. Its incorporation into the chemical structure of a molecule can impart desirable properties such as enhanced biological activity or improved pharmacokinetic profiles. Furthermore, in the field of materials science, this compound can be employed to synthesize functional materials with specific electronic or optical properties. Its role in chemical synthesis extends to catalysis, where it can act as a catalyst or a ligand in various reactions, facilitating the formation of complex molecular structures. Overall, the application of 4-Amino-N-[2-(diethylamino)ethyl]benzamide monohydrochloride in chemical synthesis underscores its significance in advancing research and development across diverse industrial sectors.