structure of tert-Butyl octahydro-1,5-naphthyridine-1(2H)-carboxylate

tert-Butyl octahydro-1,5-naphthyridine-1(2H)-carboxylate

CAS No.: 1000931-58-7
M. Wt: 240.34200
M. Fa: C13H24N2O2
InChI Key: NJASRKUXYJXBNQ-UHFFFAOYSA-N
Appearance: colorless or yellow liquid

Names and Identifiers of 1000931-58-7

CAS Number

1000931-58-7

IUPAC Name

tert-butyl 3,4,4a,5,6,7,8,8a-octahydro-2H-1,5-naphthyridine-1-carboxylate

InChI

InChI=1S/C13H24N2O2/c1-13(2,3)17-12(16)15-9-5-6-10-11(15)7-4-8-14-10/h10-11,14H,4-9H2,1-3H3

InChIKey

NJASRKUXYJXBNQ-UHFFFAOYSA-N

Canonical SMILES

CC(C)(C)OC(=O)N1CCCC2C1CCCN2

Physical and chemical properties of 1000931-58-7

Exact Mass

240.18400

LogP

2.40460

Molecular Formula

C13H24N2O2

Molecular Weight

240.34200

PSA

41.57000

Safety Information of 1000931-58-7

Pictograms

Signal Word

Warning

Safety Data Sheet

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

Applications of 1000931-58-7

The applications of 1-BOC-decahydro-1,5-naphthyridine span various fields:

  • Pharmaceuticals: As a building block in drug design due to its biological activity and ability to interact with biological targets.
  • Material Science: Used in developing polymers and materials with specific properties due to its unique structural features.
  • Chemical Research: Employed as an intermediate in synthesizing more complex organic molecules.

Interaction Studies of 1000931-58-7

Interaction studies involving 1-BOC-decahydro-1,5-naphthyridine focus on its binding affinity with various biological targets. Notably:

  • Neurokinin Receptors: Research has shown that certain derivatives exhibit binding properties that may lead to therapeutic applications in treating neurological disorders.
  • Enzyme Inhibition: Studies indicate potential for inhibiting specific enzymes involved in metabolic pathways, showcasing its relevance in drug development.

Biological Activity of 1000931-58-7

Research indicates that derivatives of naphthyridines exhibit significant biological activities, including:

  • Anticancer Properties: Some studies have suggested that naphthyridine derivatives can inhibit tumor growth by acting on specific cellular pathways.
  • Antimicrobial Activity: Compounds similar to 1-BOC-decahydro-1,5-naphthyridine have shown effectiveness against various bacterial strains.
  • Receptor Antagonism: Certain derivatives have been identified as potential antagonists for neurokinin receptors, indicating their role in neurological applications.