Cat. No JK955952_100_G
J&K Chemical

Product Information

Product Name
3-Quinuclidinone hydrochloride, 99%, extra pure
Brand Name
J&K
Product Number
955952
CAS
1193-65-3
SDS Document
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
102019
IUPAC Name
1-azabicyclo2.2.2octan-3-one;hydrochloride
InChI Key
RFDPHKHXPMDJJD-UHFFFAOYSA-N
SMILES
C1CN2CCC1C(=O)C2.Cl

Safety Information

Storage Condition
Store at 2-8℃

Description

3-Quinuclidinone hydrochloride is widely used in the following fields:

  1. Pharmaceutical Synthesis Intermediate

    • Serves as a key chiral building block for synthesizing anticholinergic drugs (e.g., asthma medications, anti-Parkinson's agents).

  2. Neuroscience Research

    • Used in the preparation of ligands or probe molecules targeting muscarinic acetylcholine receptors (mAChRs).

  3. Pesticide Development

    • Acts as an active molecular scaffold for novel insecticides or fungicides.

  4. Organic Methodology Studies

    • Employed as a model substrate for developing new asymmetric catalysis or green synthesis methods.

  5. Analytical Chemistry

    • Functions as a derivatization reagent or internal standard in gas chromatography or mass spectrometry analysis.

References Data Source From Pubchem

Poly(aryl N-methyl quinuclidinium) anion exchange membrane with both ultra-high alkaline stability and dimensional stability

Publication Name: Science China Materials
Publication Date: 2024-02-02
DOI: 10.1007/s40843-023-2761-9

A pharmacophore-based approach to demonstrating the scope of alcohol dehydrogenases

Publication Name: Bioorganic & Medicinal Chemistry
Publication Date: 2023-04-01
DOI: 10.1016/j.bmc.2023.117255

Targeting organophosphorus compounds poisoning by novel quinuclidine-3 oximes: development of butyrylcholinesterase-based bioscavengers

Publication Name: Archives of Toxicology
Publication Date: 2020-06-24
DOI: 10.1007/s00204-020-02811-5

Synthesis, biological evaluation and molecular docking studies of novel quinuclidinone derivatives as potential antimicrobial and anticonvulsant agents

Publication Name: Medicinal Chemistry Research
Publication Date: 2017-05-19
DOI: 10.1007/s00044-017-1904-z

Molecular cloning and characterization of a tropinone reductase from Dendrobium nobile Lindl

Publication Name: Molecular Biology Reports
Publication Date: 2012-10-27
DOI: 10.1007/s11033-012-2156-0

3-Quinuclidinone hydrochloride, 99%, extra pure

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