879403-42-6 | (S)-N-Boc-2-aminomethylmorpholine

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$12.00	$9.00
250mg	95%	in stock	$23.00	$17.00
1g	95%	in stock	$65.00	$46.00
5g	95%	in stock	$213.00	$150.00
25g	95%	in stock	$1,064.00	$745.00

Description

• Catalog Number: AB47935
• Chemical Name: (S)-N-Boc-2-aminomethylmorpholine
• CAS Number: 879403-42-6
• Molecular Formula: C10H20N2O3
• Molecular Weight: 216.2774
• MDL Number: MFCD11707017
• SMILES: NC[C@@H]1OCCN(C1)C(=O)OC(C)(C)C

Computed Properties

• Complexity: 225
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• XLogP3: -0.1

Upstream Synthesis Route

(S)-4-Boc-2-aminomethylmorpholine is a versatile compound that finds numerous applications in chemical synthesis, particularly in the field of organic chemistry. This compound with a Boc (tert-butoxycarbonyl) protecting group on the nitrogen atom and a morpholine ring structure offers unique reactivity and selectivity in various reactions.One key application of (S)-4-Boc-2-aminomethylmorpholine is as a chiral building block in the synthesis of pharmaceuticals and agrochemicals. Its chiral nature allows for the preparation of enantiopure compounds, which are crucial in drug development to ensure high efficacy and minimal side effects. By incorporating (S)-4-Boc-2-aminomethylmorpholine into the molecular structure of a target compound, chemists can control the stereochemistry of the final product, leading to improved biological activity.Additionally, this compound is widely used in asymmetric synthesis, where its chirality imparts stereocontrol to reactions, enabling the selective formation of single enantiomers over racemic mixtures. This is particularly important in the production of fine chemicals and advanced materials where stereoselectivity is essential for their properties and functions.Furthermore, (S)-4-Boc-2-aminomethylmorpholine serves as a versatile intermediate in the preparation of complex molecules such as peptides, amino acids, and heterocycles. Its Boc-protected amine group can undergo various transformations, including deprotection and functional group manipulations, to introduce desired functionalities into target molecules.In summary, the unique properties of (S)-4-Boc-2-aminomethylmorpholine make it a valuable tool in the synthesis of chiral compounds with applications spanning from pharmaceuticals to materials science. Its role in enabling stereocontrol and functional group manipulation underscores its significance in modern organic synthesis.