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TCI

CAS 181140-34-1

(R)-N-Glycidylphthalimide TCI G0327

(R)-N-Glycidylphthalimide TCI G0327

Chemical Identity

Other names
(R)-N-(2,3-Epoxypropyl)phthalimide
CAS No.
181140-34-1
PubChem
CID 719415·SID 87560476
Formula
C11H9NO3
Molecular weight
203.20 g/mol
Purity
>99.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-[[(2R)-oxiran-2-yl]methyl]isoindole-1,3-dione
SMILES
C1C(O1)CN2C(=O)C3=CC=CC=C3C2=O
InChIKey
DUILGEYLVHGSEE-SSDOTTSWSA-N
MDL
MDL04973349
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(R)-N-Glycidylphthalimide is a chiral building block widely used in asymmetric synthesis to construct molecules with optical activity. This compound plays a critical role in organic chemistry research, particularly in the development of bioactive compounds. Its unique structure enables selective and specific chemical reactions, making it an essential tool for chemists working on complex molecular synthesis. As a chiral molecule, it is highly valued for its ability to influence the stereochemistry of target compounds, which is crucial in pharmaceutical and food chemistry applications.

The compound's chiral nature and reactive functional groups make it a preferred choice for researchers aiming to create enantiomerically pure products. Its ability to interact with various reagents allows for the synthesis of a wide range of derivatives with tailored properties. The structural complexity of (R)-N-Glycidylphthalimide also supports high selectivity in chemical transformations, which is vital for achieving desired outcomes in synthetic processes. This makes it a versatile and reliable reagent in advanced chemical research.

In Indonesian laboratories, (R)-N-Glycidylphthalimide is commonly used by chemists, pharmacologists, and biochemists for research and development purposes. It is particularly relevant in studies involving the synthesis of bioactive compounds and the analysis of complex molecular structures. Its application is widespread in academic and industrial settings where precision and control over stereochemistry are essential. The compound is a key component in the pursuit of more effective and safer pharmaceuticals.

TCI brochures (PDF)

  • Asymmetric Synthesis: This compound is ideal for creating enantiomerically pure compounds, which is essential in pharmaceutical research for developing more effective and safer drugs.
  • Bioactive Compound Development: Its chiral structure enables the synthesis of molecules with specific biological activities, making it valuable in drug discovery and development.
  • Molecular Structure Analysis: The compound's reactivity and stereochemistry make it useful in studying complex molecular interactions and structural properties.
  • Organic Chemistry Research: It is frequently used in synthetic pathways that require precise control over stereochemical outcomes, supporting advanced chemical investigations.
  • Food Chemistry Applications: Its role in creating chiral molecules is relevant in the development of food additives and flavor compounds with specific properties.

Brand TCI
CAS number 181140-34-1
Molecular formula —
Purity —
Category Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes Available in various quantities as per supplier specifications
Physical form Solid
Storage Store in a cool, dry place away from moisture and light

(R)-N-Glycidylphthalimide should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep the compound in a tightly sealed container to prevent exposure to moisture and air. Due to its reactive nature, it should be handled with care using appropriate personal protective equipment. Storage away from incompatible substances is essential to avoid any chemical interactions. Proper labeling of containers is necessary for safe handling and to ensure the compound remains uncontaminated. Regular inspection of storage conditions ensures the compound remains suitable for use in laboratory applications.

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