(R)-1-(tert-Butoxycarbonyl)-2-azetidinemethanol TCI B2174

Chemical Identity

CAS No.: 161511-90-6
PubChem: CID 11074142·SID 87565035
Formula: C9H17NO3
Molecular weight: 187.24 g/mol
Purity: >98.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: tert-butyl (2R)-2-(hydroxymethyl)azetidine-1-carboxylate
SMILES: CC(C)(C)OC(=O)N1CC[C@@H]1CO
InChIKey: XIRUXUKRGUFEKC-SSDOTTSWSA-N

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(R)-1-(tert-Butoxycarbonyl)-2-azetidinemethanol is a chiral building block widely used in asymmetric synthesis to construct molecules with optical activity. This compound plays a crucial role in chemical laboratories, particularly in the field of chiral synthesis where precise control over molecular structure is essential. Its unique azetidine ring structure enables complex and specific chemical reactions, making it a valuable tool for researchers working on advanced organic synthesis.

The compound's chiral nature and stability under specific conditions make it a preferred choice for laboratory applications. Its ability to participate in asymmetric reactions allows for the efficient synthesis of enantiomerically pure compounds, which are critical in pharmaceutical and biochemical research. Additionally, its availability in crystalline or solid form simplifies handling and processing, enhancing its usability in various experimental setups.

In Indonesian laboratories, this compound is frequently used by chemists and pharmacologists involved in research related to the synthesis of active compounds. It is an essential component in the development of new therapeutic agents, particularly in pharmacology and biochemistry. Its role in creating bioactive molecules makes it a key material in both academic and industrial research environments.

TCI brochures (PDF)

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

Related TCI products

Chiral Synthesis: This compound is ideal for creating enantiomerically pure compounds, essential in pharmaceutical research for drug development.
Organic Chemistry Research: Its unique structure supports complex reactions, making it a staple in synthetic chemistry experiments.
Bioactive Compound Development: Used in the synthesis of bioactive molecules, it plays a key role in drug discovery and development.
Asymmetric Catalysis Studies: Its chiral nature allows for precise control in asymmetric catalytic processes, enhancing reaction selectivity.
Academic Research Projects: Widely utilized in Indonesian universities and research institutions for teaching and experimental work.

Brand	TCI
CAS number	161511-90-6
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid or crystalline
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 purity. It is recommended to use airtight containers to prevent exposure to air and contaminants. Due to its chiral nature, it is important to handle it with care to avoid contamination or degradation. Proper labeling and storage conditions are essential to ensure its effectiveness in laboratory applications. Always follow standard safety protocols when handling chemical substances to ensure a safe working environment.

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