(S,S)-2,2'-Isopropylidenebis(4-isopropyl-2-oxazoline) TCI I1051

Chemical Identity

CAS No.: 131833-92-6
PubChem: CID 11821563·SID 468592070
Formula: C15H26N2O2
Molecular weight: 266.38 g/mol
Purity: >98.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (4S)-4-propan-2-yl-2-[2-[(4S)-4-propan-2-yl-4,5-dihydro-1,3-oxazol-2-yl]propan-2-yl]-4,5-dihydro-1,3-oxazole
SMILES: CC(C)[C@H]1COC(=N1)C(C)(C)C2=N[C@H](CO2)C(C)C
InChIKey: XFZUPCITFHSROM-VXGBXAGGSA-N

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Berat 250mg 1g

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(3 paragraphs. Paragraph 1 AT LEAST 70 words: what this material/instrument is and its role in the laboratory. Paragraph 2 AT LEAST 70 words: the properties that make it a preferred choice. Paragraph 3 AT LEAST 60 words: typical use context in Indonesian laboratories.)

The TCI I1051 131833-92-6 (S,S)-2,2'-Isopropylidenebis(4-isopropyl-2-oxazoline) is a chiral reagent used in asymmetric synthesis to produce compounds with specific stereochemical configurations. This compound plays a crucial role in the development of pharmaceuticals and fine chemicals by enabling the selective formation of enantiomers. Its application is essential in laboratories where precision in molecular structure is required to achieve desired biological activities. As a chiral building block, it supports the synthesis of complex molecules with high enantioselectivity, making it a valuable tool in modern synthetic chemistry.

This reagent is preferred due to its high chiral purity and stability under standard laboratory conditions. Its molecular structure allows for efficient participation in catalytic processes, enhancing reaction yields and reducing byproduct formation. The (S,S) configuration ensures consistent stereochemical outcomes, which is vital for applications in drug development and organic synthesis. Its compatibility with various reaction conditions and solvents further contributes to its widespread use in both academic and industrial research settings.

In Indonesian laboratories, this compound is commonly used in pharmaceutical and chemical research institutions. It is particularly relevant in the development of new drugs and bioactive compounds, where controlling stereochemistry is critical. Its application supports local research efforts in creating innovative chemical products and advancing scientific knowledge in the field of asymmetric synthesis.

TCI brochures (PDF)

Chiral Ligands 2024-12-13 · p. 3
Ligands 2025-12-01 · p. 3

Related TCI products

Asymmetric synthesis is a key application where this chiral reagent enables the selective formation of enantiomers, crucial for pharmaceutical development.
Organic chemistry research benefits from its use in creating complex molecules with specific stereochemical configurations, enhancing product purity and efficacy.
Drug discovery programs rely on this compound to develop new therapeutics with improved bioavailability and reduced side effects.
Academic research institutions use it to explore novel synthetic pathways and improve reaction efficiency in chiral catalysis.
Industrial chemical production employs it to manufacture high-purity compounds for use in various applications, including agrochemicals and specialty chemicals.

Brand	TCI
CAS number	131833-92-6
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Catalysts, Chiral Ligands, Chiral Reagents
Pack sizes	Available in various sizes as per supplier specifications
Physical form	Solid or powder, depending on the formulation
Storage	—

This compound should be stored in a cool, dry, and well-ventilated area away from direct sunlight. It is recommended to use airtight containers to prevent moisture absorption and maintain its chemical integrity. Due to its chiral nature, it should be handled with care to avoid contamination. Proper labeling and storage conditions are essential to ensure its stability and effectiveness in laboratory applications. Always follow standard safety protocols when handling chemical reagents to ensure a safe working environment.

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