1187929-79-8 | (S)-tert-Butyl 3-(aminomethyl)morpholine-4-carboxylate

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$48.00	$34.00
250mg	97%	in stock	$73.00	$52.00
1g	97%	in stock	$280.00	$196.00

Description

• Catalog Number: AE09174
• Chemical Name: (S)-tert-Butyl 3-(aminomethyl)morpholine-4-carboxylate
• CAS Number: 1187929-79-8
• Molecular Formula: C10H20N2O3
• Molecular Weight: 216.2774
• MDL Number: MFCD06796250
• SMILES: NC[C@H]1COCCN1C(=O)OC(C)(C)C

Upstream Synthesis Route

(S)-tert-Butyl 3-(aminomethyl)morpholine-4-carboxylate, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound serves as a valuable building block in the creation of various organic molecules due to its unique structural properties and reactivity.One key application of (S)-tert-Butyl 3-(aminomethyl)morpholine-4-carboxylate is its use as a chiral ligand in asymmetric synthesis. By incorporating this compound into a reaction system, chemists can promote enantioselective transformations, leading to the production of optically pure compounds. This is particularly significant in the pharmaceutical industry, where the chirality of a molecule can greatly impact its biological activity and pharmacological properties.Furthermore, (S)-tert-Butyl 3-(aminomethyl)morpholine-4-carboxylate can also act as a protecting group for amines in organic synthesis. By strategically installing and removing this protective group during a synthetic sequence, chemists can control the reactivity and selectivity of amine-containing intermediates, facilitating the construction of complex molecular structures with precision.Overall, the versatile nature of (S)-tert-Butyl 3-(aminomethyl)morpholine-4-carboxylate makes it a valuable tool in the hands of synthetic chemists, enabling the efficient and controlled assembly of diverse organic compounds with specific stereochemical and functional group arrangements.