9-Boc-7-oxa-9-azabicyclo[3.3.1]nonan-3-one - CAS 280761-97-9

9-Boc-7-oxa-9-azabicyclo[3.3.1]nonan-3-one - CAS 280761-97-9 Catalog number: BADC-01581

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9-Boc-7-oxa-9-azabicyclo[3.3.1]nonan-3-one (CAS# 280761-97-9) is a useful research chemical.

Category
ADCs Linker
Product Name
9-Boc-7-oxa-9-azabicyclo[3.3.1]nonan-3-one
CAS
280761-97-9
Catalog Number
BADC-01581
Molecular Formula
C12H19NO4
Molecular Weight
241.28
9-Boc-7-oxa-9-azabicyclo[3.3.1]nonan-3-one

Ordering Information

Catalog Number Size Price Quantity
BADC-01581 -- $-- Inquiry
Description
9-Boc-7-oxa-9-azabicyclo[3.3.1]nonan-3-one (CAS# 280761-97-9) is a useful research chemical.
Synonyms
7-oxo-3-oxa-9-aza-bicyclo[3.3.1]nonane-9-carboxylic acid tert-butyl ester
IUPAC Name
tert-butyl 7-oxo-3-oxa-9-azabicyclo[3.3.1]nonane-9-carboxylate
Canonical SMILES
CC(C)(C)OC(=O)N1C2CC(=O)CC1COC2
InChI
InChI=1S/C12H19NO4/c1-12(2,3)17-11(15)13-8-4-10(14)5-9(13)7-16-6-8/h8-9H,4-7H2,1-3H3
InChIKey
CQLVVTNYEYTHMM-UHFFFAOYSA-N
LogP
1.29170
Appearance
White Solid
Signal Word
Warning

9-Boc-7-oxa-9-azabicyclo[3.3.1]nonan-3-one, a synthetic organic compound with diverse biochemical applications, is featured in the following four key areas presented with high perplexity and burstiness:

Pharmaceutical Synthesis: Serving as a pivotal intermediate in the synthesis of intricate pharmaceutical compounds, 9-Boc-7-oxa-9-azabicyclo[3.3.1]nonan-3-one plays a crucial role in constructing molecular frameworks essential for new drug development. Its distinct bicyclic structure offers a robust scaffold for further functionalization and optimization of pharmacological properties, paving the way for innovative drug discovery and design.

Medicinal Chemistry: Widely utilized in medicinal chemistry, this compound is instrumental in the design and synthesis of novel therapeutic agents. Researchers harness its adaptability to create analogs that boost biological activity or diminish side effects. Leveraging its rigidity and steric properties, scientists craft compounds targeting various therapeutic areas, from central nervous system disorders to infectious diseases, showcasing its versatility and potential impact on drug development.

Catalyst Development: Exploring new frontiers in catalysis, 9-Boc-7-oxa-9-azabicyclo[3.3.1]nonan-3-one emerges as a chiral auxiliary or ligand in asymmetric synthesis. Its unique structural attributes facilitate the formation of chiral centers, a critical aspect in generating enantiomerically pure compounds. This application holds significance in producing high-value chemicals with precise stereochemistry, underscoring the compound's pivotal role in advancing catalytic processes.

Chemical Biology: Delving into the realm of chemical biology, researchers utilize 9-Boc-7-oxa-9-azabicyclo[3.3.1]nonan-3-one as a molecular tool to probe intricate biological systems. Acting as a valuable asset for studying enzyme binding sites and protein interactions, this compound enables scientists to dissect complex biological pathways and unravel the molecular underpinnings of cellular processes. By incorporating it into probes or inhibitors, researchers gain insights into fundamental biological mechanisms, highlighting its significance in driving forward our understanding of cellular functions.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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