(R)-3-(Aminomethyl)-1-(tert-butoxycarbonyl)pyrrolidine TCI A3285

Chemical Identity

CAS No.: 199174-29-3
PubChem: CID 1515152·SID 468590215
Formula: C10H20N2O2
Molecular weight: 200.28 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: tert-butyl (3R)-3-(aminomethyl)pyrrolidine-1-carboxylate
SMILES: CC(C)(C)OC(=O)N1CC[C@@H](C1)CN
InChIKey: OGCCBDIYOAFOGK-MRVPVSSYSA-N

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(R)-3-(Aminomethyl)-1-(tert-butoxycarbonyl)pyrrolidine is a chemical compound widely used in laboratory settings for the synthesis of heterocyclic compounds. This building block plays a crucial role in organic chemistry by providing a stable and reactive structure that supports complex molecular transformations. Its unique combination of aminomethyl and tert-butoxycarbonyl groups makes it highly versatile for various synthetic routes. In research laboratories, it is a key reagent for constructing molecules with specific functional groups and stereochemistry.

The compound is valued for its molecular stability and moderate reactivity, which allows it to participate in a range of chemical reactions such as reduction, hydrolysis, and substitution. The presence of the tert-butoxycarbonyl group also makes it an effective protecting group, offering control over reaction selectivity and preventing unwanted side reactions. This feature is particularly important in multi-step syntheses where precise control is necessary. Its compatibility with a variety of reaction conditions further enhances its utility in both academic and industrial research.

In Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in the development of new compounds with potential applications in medicine and materials science. Its availability in user-friendly packaging makes it a practical choice for researchers seeking reliable and consistent results. The compound's role in advancing chemical synthesis makes it a valuable asset in the pursuit of scientific innovation.

Related TCI products

Organic synthesis of heterocyclic compounds due to its stable molecular structure and functional group versatility.
Protection of amino groups in complex molecule synthesis through the tert-butoxycarbonyl group.
Development of pharmaceutical compounds in medicinal chemistry applications requiring controlled reactivity.
Research in material science for the creation of advanced polymers and functional materials.
Support for academic research in chemical engineering and synthetic chemistry laboratories.

Brand	TCI
CAS number	199174-29-3
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic 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 direct sunlight and moisture

This compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a tightly sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood. Avoid contact with strong acids or bases to prevent unwanted chemical reactions. Always use appropriate personal protective equipment, such as gloves and safety goggles, when handling the compound. Proper storage and handling ensure the compound remains effective and safe for use in laboratory applications.

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