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CAS 123536-14-1

(R)-(+)-3-Aminoquinuclidine Dihydrochloride TCI A2830

(R)-(+)-3-Aminoquinuclidine Dihydrochloride TCI A2830

Chemical Identity

CAS No.
123536-14-1
PubChem
CID 12494972·SID 253660723
Formula
C7H16Cl2N2
Molecular weight
199.12 g/mol
Purity
>98.0%(N)(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(3R)-1-azabicyclo[2.2.2]octan-3-amine;dihydrochloride
SMILES
C1CN2CCC1[C@H](C2)N.Cl.Cl
InChIKey
STZHBULOYDCZET-KLXURFKVSA-N
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(R)-(+)-3-Aminoquinuclidine Dihydrochloride is a chiral compound widely used in asymmetric synthesis, playing a crucial role in the development of chiral molecules with specific biological activity. This compound is essential in organic chemistry research, particularly in pharmaceutical and medicinal chemistry applications. Its unique stereochemical properties make it a valuable tool for creating enantiomerically pure compounds, which are critical in drug development and other advanced chemical processes. As a chiral building block, it provides a foundation for synthesizing complex molecules with precise stereochemistry.

The compound is known for its stability under standard laboratory conditions and its solubility in organic solvents, which simplifies handling and manipulation during chemical reactions. These properties make it a preferred choice for researchers working on asymmetric synthesis and chiral compound development. Its ability to participate in controlled stereoselective reactions enhances its utility in creating compounds with desired biological effects. The compound's reliability and consistent performance contribute to its popularity in both academic and industrial research settings.

In Indonesian laboratories, (R)-(+)-3-Aminoquinuclidine Dihydrochloride is commonly used in pharmaceutical and organic chemistry research. Researchers in universities and research institutions rely on this compound for experiments requiring precise stereochemical control. Its application is widespread in drug discovery and development, where the synthesis of chiral molecules is essential for creating effective and safe pharmaceutical products.

TCI brochures (PDF)

  • Asymmetric synthesis in pharmaceutical research due to its chiral structure and stereoselective properties.
  • Development of enantiomerically pure compounds for drug discovery and medicinal chemistry applications.
  • Organic chemistry experiments requiring controlled stereochemistry in complex molecule synthesis.
  • Research in pharmacology where chiral compounds are essential for biological activity studies.
  • Creation of chiral building blocks for the synthesis of biologically active molecules in academic and industrial settings.

Brand TCI
CAS number 123536-14-1
Molecular formula —
Purity —
Category Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes Available in various quantities as per supplier specifications
Physical form Solid powder
Storage Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its stability and purity. It is recommended to use airtight containers to prevent exposure to humidity and contaminants. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. While it is generally stable under standard conditions, it should be kept in a secure location to prevent accidental exposure. Proper storage and handling are essential to maintain its effectiveness in research applications.

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