[2-oxo-2-[3-[3-(piperidin-1-ylmethyl)phenoxy]propylamino]ethyl] acetate;hydrochloride


Chemical Name: [2-oxo-2-[3-[3-(piperidin-1-ylmethyl)phenoxy]propylamino]ethyl] acetate;hydrochloride
CAS Number: 93793-83-0
Product Number: AG0038J2(AGN-PC-0JL1JQ)
Synonyms:
MDL No: MFCD00941429
Molecular Formula: C19H29ClN2O4
Molecular Weight: 384.8976

Identification/Properties


Computed Properties
Molecular Weight:
384.901g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
10
Exact Mass:
384.182g/mol
Monoisotopic Mass:
384.182g/mol
Topological Polar Surface Area:
67.9A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
410
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



The compound 2-Acetoxy-N-[3-[3-(1-piperidinomethylphenoxy]propyl]acetamide hydrochloride holds great importance in chemical synthesis due to its versatile applications. This complex compound is commonly used as a reagent in reactions that involve the formation of amide bonds. It serves as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and organic compounds.In chemical synthesis, 2-Acetoxy-N-[3-[3-(1-piperidinomethylphenoxy]propyl]acetamide hydrochloride acts as a catalyst for amidation reactions, facilitating the coupling of amine and carboxylic acid functional groups to form stable amide linkages. This compound is particularly valued for its ability to promote selective amide bond formation under mild reaction conditions, making it a valuable tool in the development of novel molecules in the pharmaceutical and chemical industries.Moreover, the unique structural properties of 2-Acetoxy-N-[3-[3-(1-piperidinomethylphenoxy]propyl]acetamide hydrochloride enable it to participate in diverse synthetic pathways, allowing for the efficient construction of complex molecular frameworks. Its compatibility with a wide range of functional groups makes it a versatile building block for the synthesis of complex organic molecules with specific biological activities.Overall, the application of 2-Acetoxy-N-[3-[3-(1-piperidinomethylphenoxy]propyl]acetamide hydrochloride in chemical synthesis offers a reliable and efficient solution for the construction of intricate molecular structures, making it an indispensable tool for researchers and chemists in the development of new compounds with targeted properties.