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TCI

CAS 59025-03-5

(-)-O-Acetyl-L-malic Anhydride TCI A1101

(-)-O-Acetyl-L-malic Anhydride TCI A1101

Chemical Identity

CAS No.
59025-03-5
PubChem
CID 11126528·SID 87562587
Formula
C6H6O5
Molecular weight
158.11 g/mol
Purity
>97.0%(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
[(3S)-2,5-dioxooxolan-3-yl] acetate
SMILES
CC(=O)O[C@H]1CC(=O)OC1=O
InChIKey
SSWJHSASZZAIAU-BYPYZUCNSA-N
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(-)-O-Acetyl-L-malic Anhydride is a chiral chemical compound widely used in asymmetric synthesis to construct molecules with specific stereochemistry and biological activity. This reagent plays a vital role in organic laboratories where precise control over molecular structure is essential. Its unique chiral nature allows chemists to produce enantiomerically pure compounds, which are critical in pharmaceutical and biochemical research. As a building block in complex syntheses, it enables the creation of compounds with defined stereochemical configurations, enhancing the efficiency of drug development and molecular analysis.

The compound’s anhydride structure and reactivity make it a preferred choice for synthetic chemists. It readily reacts with alcohols, amines, and acids, facilitating the formation of esters, amides, and other functional groups. The absence of water in its structure simplifies reaction conditions, reducing the risk of side reactions. Its stability under controlled laboratory conditions further enhances its reliability as a reagent. These properties collectively make it a versatile and efficient tool for synthetic chemists working in both academic and industrial settings.

In Indonesian laboratories, (-)-O-Acetyl-L-malic Anhydride is commonly used in organic chemistry research, particularly in projects involving the synthesis of optically active compounds. It is frequently found in studies related to drug development, molecular structure analysis, and the investigation of chiral reactivity. Its role in creating compounds with specific stereochemistry is crucial for advancing pharmaceutical and biochemical research in the region.

TCI brochures (PDF)

  • Asymmetric Synthesis: This compound is ideal for creating enantiomerically pure compounds, essential in drug development and bioactive molecule synthesis.
  • Organic Chemistry Research: It supports the synthesis of complex molecules with defined stereochemistry, enhancing the accuracy of chemical experiments.
  • Pharmaceutical Development: Its chiral nature makes it valuable for producing compounds with specific biological activities required in new drug formulations.
  • Structural Analysis: It is used in the study of molecular reactivity and stereochemistry, aiding in the understanding of chiral compound behavior.
  • Biochemical Studies: It contributes to research on enzyme interactions and molecular recognition, supporting advancements in biotechnology.

Brand TCI
CAS number 59025-03-5
Molecular formula —
Purity —
Category Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes Available in various quantities as per supplier specifications
Physical form Solid anhydride
Storage Store in a cool, dry place away from moisture and light

This compound should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which can affect its reactivity. Due to its anhydride nature, it should be handled with care to avoid contact with water or moisture. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling the compound. It should be stored in a well-ventilated area to ensure safe working conditions. Proper storage and handling are essential to preserve its effectiveness and ensure safe laboratory practices.

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