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CAS 50622-09-8

(+)-2,3-O-Isopropylidene-L-threitol TCI I0376

(+)-2,3-O-Isopropylidene-L-threitol TCI I0376

Chemical Identity

CAS No.
50622-09-8
PubChem
CID 785242·SID 87571729
Formula
C7H14O4
Molecular weight
162.18 g/mol
Purity
>97.0%(GC)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
[(4S,5S)-5-(hydroxymethyl)-2,2-dimethyl-1,3-dioxolan-4-yl]methanol
SMILES
CC1(O[C@H]([C@@H](O1)CO)CO)C
InChIKey
INVRLGIKFANLFP-WDSKDSINSA-N
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(+)-2,3-O-Isopropylidene-L-threitol is a chiral building block widely used in asymmetric synthesis to construct molecules with specific biological activities. This compound plays a crucial role in the development of pharmaceuticals and organic chemistry research by enabling the creation of enantiomerically pure compounds. Its importance lies in its ability to influence the stereochemistry of target molecules, which is essential for achieving desired pharmacological effects. In the laboratory, it is a key component for researchers aiming to explore the complexities of molecular structure and function.

The compound’s optically active nature and stable isopropylidene group make it a preferred choice for synthetic chemists. These properties allow for controlled reactions under specific conditions, enhancing the efficiency of synthetic pathways. Its chiral character ensures that the resulting products maintain the necessary stereochemistry for biological activity. This makes it a valuable tool in the synthesis of complex molecules that require precise stereochemical control. Its structural complexity also supports its use in advanced research applications.

In Indonesian laboratories, (+)-2,3-O-Isopropylidene-L-threitol is commonly used in scientific research, particularly in organic chemistry and pharmacology. It is a fundamental reagent for experiments involving asymmetric synthesis and the development of new drug candidates. Its availability and reliability make it an essential material for both academic and industrial research settings in Indonesia.

  • Asymmetric synthesis is a key application where this compound enables the creation of enantiomerically pure molecules, essential for drug development and biological activity studies.
  • Organic chemistry research benefits from its chiral structure, allowing for the synthesis of complex molecules with specific stereochemical configurations.
  • Pharmaceutical development relies on this compound to produce compounds with desired biological effects, enhancing the efficacy of drug candidates.
  • Academic research in pharmacology uses it to study molecular interactions and the impact of stereochemistry on biological responses.
  • Industrial applications in chemical synthesis leverage its stability and reactivity to design efficient and selective synthetic routes.

Brand TCI
CAS number 50622-09-8
Molecular formula —
Purity —
Category Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid
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 integrity. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its chemical properties. In a laboratory setting, it is important to handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. It should be kept in a secure location, away from incompatible substances to ensure safety. Proper labeling of storage containers is essential for easy identification and safe handling. Regular monitoring of storage conditions ensures that the compound remains in optimal condition for use in research applications.

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