structure of Pentanamide, 5-hydroxy-

Pentanamide, 5-hydroxy-

CAS No.: 29686-12-2
M. Wt: 117.14600
M. Fa: C5H11NO2
InChI Key: UYOWQFWKDDJSLV-UHFFFAOYSA-N
Appearance: White Solid

Names and Identifiers of Pentanamide, 5-hydroxy-

CAS Number

29686-12-2

EC Number

823-363-4

MDL Number

MFCD00025539

IUPAC Name

5-hydroxypentanamide

InChI

InChI=1S/C5H11NO2/c6-5(8)3-1-2-4-7/h7H,1-4H2,(H2,6,8)

InChIKey

UYOWQFWKDDJSLV-UHFFFAOYSA-N

Canonical SMILES

C(CCO)CC(=O)N

UNII

62Z3TLQ3UB

UNSPSC Code

12352100

Physical and chemical properties of Pentanamide, 5-hydroxy-

Boiling Point

333.5ºC at 760 mmHg

Density

1.071g/cm3

Exact Mass

117.07900

Flash Point

155.5ºC

H Bond Acceptors

2

H Bond Donors

2

Index of Refraction

1.466

LogP

0.33460

Molecular Formula

C5H11NO2

Molecular Weight

117.14600

PSA

63.32000

Vapour Pressure

9.69E-06mmHg at 25°C

Safety Information of Pentanamide, 5-hydroxy-

Pictograms

Signal Word

 Warning

Safety Data Sheet
Supports customized editing of SDS information and downloading in PDF documents.

Applications of Pentanamide, 5-hydroxy-

5-Hydroxypentanamide has several applications across different fields:

  • Medicinal Chemistry: Due to its neuropharmacological potential, it may serve as a lead compound for developing new therapeutic agents targeting neurological disorders.
  • Organic Synthesis: The compound can act as an intermediate in synthesizing more complex organic molecules due to its reactive functional groups.

Interaction Studies of Pentanamide, 5-hydroxy-

Studies on the interactions of 5-hydroxypentanamide with various biomolecules have highlighted its capacity to form hydrogen bonds. This property enhances its binding affinity to proteins and receptors involved in neurotransmission, which is crucial for understanding its mechanism of action as a potential therapeutic agent.

Biological Activity of Pentanamide, 5-hydroxy-

Research indicates that 5-hydroxypentanamide exhibits potential biological activities. It has been studied for its role as an inhibitor of gamma-aminobutyric acid transporters, which are crucial for regulating neurotransmitter levels in the brain. The compound's ability to form hydrogen bonds due to its hydroxyl and amide groups enhances its interaction with biological targets, making it a candidate for neuropharmacological applications.

Physical sample testing spectrum (NMR) of Pentanamide, 5-hydroxy-

Physical sample testing spectrum (NMR) of Pentanamide, 5-hydroxy-

Retrosynthesis analysis of Pentanamide, 5-hydroxy-

  • Route#1

    Cas:542-28-9
    Cas:29686-12-2

  • Route#2

    Cas:2427-16-9
    Cas:29686-12-2