(R,R,R)-Triglycidyl Isocyanurate TCI I0580

Chemical Identity

CAS No.: 240408-78-0
PubChem: CID 198383·SID 87571923
Formula: C12H15N3O6
Molecular weight: 297.26 g/mol
Purity: >95.0%(HPLC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 1,3,5-tris[[(2R)-oxiran-2-yl]methyl]-1,3,5-triazinane-2,4,6-trione
SMILES: C1[C@H](O1)CN2C(=O)N(C(=O)N(C2=O)C[C@@H]3CO3)C[C@@H]4CO4
InChIKey: OUPZKGBUJRBPGC-IWSPIJDZSA-N

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(R,R,R)-Triglycidyl Isocyanurate is a chiral compound widely used in asymmetric synthesis to construct complex molecular structures. It plays a crucial role in chemical laboratories where precise control over stereochemistry is essential. This material is particularly valuable in organic chemistry research, enabling the synthesis of chiral compounds with high enantiomeric purity. Its unique molecular structure allows for specific reactivity under various reaction conditions, making it an indispensable tool for researchers working on stereoselective reactions.

The compound is known for its chemical stability and predictable reactivity, which simplifies the synthesis process in laboratory settings. Its chiral nature ensures that it can be used effectively in applications requiring stereochiral control, such as pharmaceutical development and the creation of complex organic molecules. This makes it a preferred choice for chemists aiming to achieve high selectivity and efficiency in their synthetic pathways.

In Indonesian laboratories, (R,R,R)-Triglycidyl Isocyanurate is commonly used in organic chemistry research, especially in asymmetric synthesis and the development of new compounds. It is frequently employed by research institutions and universities to meet the demands of chemical and pharmaceutical studies. Its availability in solid form facilitates easy handling and integration into various chemical reactions, enhancing its practicality in laboratory environments.

TCI brochures (PDF)

Chiral Building Blocks 2025-04-14 · p. 5

Related TCI products

Asymmetric Synthesis for the creation of complex organic compounds due to its chiral structure and stereoselective reactivity.
Pharmaceutical Development where precise stereochemical control is necessary for drug molecule synthesis.
Organic Chemistry Research for building molecular frameworks with high enantiomeric purity.
Chiral Compound Synthesis to produce enantiomerically pure substances used in various scientific applications.
Academic Research in Indonesian universities for teaching and experimental purposes in synthetic chemistry.

Brand	TCI
CAS number	240408-78-0
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	—
Physical form	Solid
Storage	Store in a cool, dry place away from moisture and direct sunlight.

This compound should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and contaminants. Due to its chiral nature, it is important to handle it with care to avoid any unintended stereochemical changes during synthesis. Proper labeling and storage conditions are essential to ensure its effectiveness in laboratory applications. Always follow standard laboratory safety protocols when handling this material to ensure safe and efficient use.

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