(S)-1-(tert-Butoxycarbonyl)-2-azetidinemethanol TCI B2123

Chemical Identity

CAS No.: 161511-85-9
PubChem: CID 10511797·SID 87564991
Formula: C9H17NO3
Molecular weight: 187.24 g/mol
Purity: >95.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

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

Rp 3.285.450,00

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(S)-1-(tert-Butoxycarbonyl)-2-azetidinemethanol is a chiral building block widely used in asymmetric synthesis to construct complex molecular structures. This compound plays a critical role in chemical laboratories, particularly in research focused on bioactive compounds. Its unique azetidine ring structure enables specific chemical reactions, making it essential for the development of pharmaceuticals and organic chemicals. Due to its structural features, it is a key component in the synthesis of enantiomerically pure compounds, which are vital in the pharmaceutical and medical research sectors.

The compound’s tert-butoxycarbonyl group enhances its chemical stability and facilitates reaction processes, making it a preferred choice for synthetic chemists. Its asymmetric nature allows for enantioselective synthesis, a process crucial for creating drugs with high efficacy and minimal side effects. Additionally, the reactivity of the azetidine ring enables a variety of chemical transformations, such as bond formation and substitution reactions. These properties make it highly versatile and valuable in both academic and industrial research settings.

In Indonesian laboratories, this compound is commonly used in chemical research, especially in asymmetric synthesis and the development of new compounds. It is frequently employed in pharmaceutical and medical research to explore the reactivity of molecules and their applications in drug development. Many research institutions and universities in Indonesia rely on this compound to advance their understanding of molecular behavior and its implications in various scientific fields.

TCI brochures (PDF)

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

Related TCI products

Asymmetric Synthesis: This compound is ideal for creating enantiomerically pure compounds, essential in pharmaceutical research for drug development.
Organic Chemistry Research: Its reactive azetidine ring and stable tert-butoxycarbonyl group make it a valuable tool for exploring new chemical reactions and molecular structures.
Bioactive Compound Development: The compound is used to synthesize compounds with biological activity, supporting research into potential therapeutic agents.
Medicinal Chemistry Studies: Its structural versatility allows for the design of complex molecules with specific pharmacological properties.
Academic Research: Widely used in Indonesian universities for teaching and research in synthetic chemistry and molecular biology.

Brand	TCI
CAS number	161511-85-9
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid or liquid, depending on the specific product variant
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. It is recommended to use airtight containers to prevent exposure to moisture and air, which could affect its reactivity. Due to its potential chemical reactivity, it should be handled in a well-ventilated laboratory setting, ideally with appropriate personal protective equipment. Avoid contact with incompatible substances to ensure safety during storage and use. Proper labeling of containers is essential for safe handling and to prevent accidental exposure. Regular inspection of storage conditions is advised to maintain optimal stability and usability of the compound.

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