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CAS 856707-74-9

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Heptanamide, 3-amino-N-cyclopropyl-2-hydroxy-, hydrochloride (1:1)

Description:
Heptanamide, 3-amino-N-cyclopropyl-2-hydroxy-, hydrochloride (1:1) is a chemical compound characterized by its amide functional group, which is derived from heptanoic acid. The presence of a cyclopropyl group contributes to its unique structural properties, while the amino and hydroxy groups suggest potential for hydrogen bonding and reactivity. As a hydrochloride salt, it is typically more soluble in water compared to its free base form, enhancing its bioavailability in pharmaceutical applications. The compound may exhibit various biological activities, potentially influencing its use in medicinal chemistry. Its molecular structure allows for interactions with biological targets, making it of interest in drug development. The specific stereochemistry and functional groups can influence its pharmacokinetics and pharmacodynamics, which are critical for therapeutic efficacy. Safety and handling considerations are essential, as with any chemical substance, particularly in laboratory or industrial settings. Overall, this compound represents a class of amides with potential applications in medicinal chemistry and pharmacology.
Formula:C10H20N2O2·ClH
InChI:InChI=1S/C10H20N2O2.ClH/c1-2-3-4-8(11)9(13)10(14)12-7-5-6-7;/h7-9,13H,2-6,11H2,1H3,(H,12,14);1H
InChI key:InChIKey=IHYTVEIDGGVQQH-UHFFFAOYSA-N
SMILES:N(C(C(C(CCCC)N)O)=O)C1CC1.Cl
Synonyms:
  • 3-Amino-N-cyclopropyl-2-hydroxyheptanamide hydrochloride
  • Heptanamide, 3-amino-N-cyclopropyl-2-hydroxy-, hydrochloride (1:1)
  • Heptanamide, 3-amino-N-cyclopropyl-2-hydroxy-, monohydrochloride
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