122709-21-1 | (S)-3-Boc-4-(methoxymethylcarbamoyl)-2,2-dimethyloxazolidine

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$49.00	$34.00
1g	95%	in stock	$55.00	$38.00
25g	95%	in stock	$1,320.00	$924.00

Description

• Catalog Number: AA24457
• Chemical Name: (S)-3-Boc-4-(methoxymethylcarbamoyl)-2,2-dimethyloxazolidine
• CAS Number: 122709-21-1
• Molecular Formula: C13H24N2O5
• Molecular Weight: 288.3401
• MDL Number: MFCD09878777
• SMILES: COCNC(=O)[C@@H]1COC(N1C(=O)OC(C)(C)C)(C)C

Computed Properties

• Complexity: 389
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 20
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• XLogP3: 1.1

Upstream Synthesis Route

(S)-tert-Butyl 4-(methoxy(methyl)carbamoyl)-2,2-dimethyloxazolidine-3-carboxylate is a valuable compound widely utilized in chemical synthesis as a chiral building block. This compound plays a crucial role in the development of stereoselective synthesis strategies in various organic reactions.One key application of (S)-tert-Butyl 4-(methoxy(methyl)carbamoyl)-2,2-dimethyloxazolidine-3-carboxylate is as a chiral auxiliary in asymmetric synthesis. By utilizing this compound, chemists can introduce chirality into a molecule, enabling the selective formation of desired enantiomers in reactions that would otherwise result in racemic mixtures. This selective control over stereochemistry is essential in the synthesis of complex natural products, pharmaceuticals, and agrochemicals.Furthermore, (S)-tert-Butyl 4-(methoxy(methyl)carbamoyl)-2,2-dimethyloxazolidine-3-carboxylate can also serve as a protecting group for amines in organic synthesis. The presence of the oxazolidine moiety allows for temporary blocking of specific amine functionalities, safeguarding them from unwanted reactions during a synthetic pathway. Subsequent deprotection of the amine group can then be achieved under mild conditions, restoring the desired functionality in the molecule.Overall, the versatile nature of (S)-tert-Butyl 4-(methoxy(methyl)carbamoyl)-2,2-dimethyloxazolidine-3-carboxylate makes it an indispensable tool in the hands of synthetic chemists, enabling precise control over stereochemistry and functional group manipulation in complex molecule construction.