1201651-31-1 | (4S)-3-{[(9H-fluoren-9-yl)methoxy]carbonyl}-2,2-dimethyl-1,3-oxazolidine-4-carboxylic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	2 weeks	$72.00	$50.00
5g	95%	2 weeks	$186.00	$130.00
10g	95%	2 weeks	$336.00	$235.00
25g	95%	2 weeks	$658.00	$460.00

Description

• Catalog Number: BM49596
• Chemical Name: (4S)-3-{[(9H-fluoren-9-yl)methoxy]carbonyl}-2,2-dimethyl-1,3-oxazolidine-4-carboxylic acid
• CAS Number: 1201651-31-1
• Molecular Formula: C21H21NO5
• Molecular Weight: 367.3951
• SMILES: OC(=O)[C@@H]1COC(N1C(=O)OCC1c2ccccc2-c2c1cccc2)(C)C

Upstream Synthesis Route

(S)-3-(((9H-Fluoren-9-yl)methoxy)carbonyl)-2,2-dimethyloxazolidine-4-carboxylic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. In organic chemistry, this compound serves as a chiral building block, providing a synthetically useful chiral center that can be incorporated into various molecules.One key application of (S)-3-(((9H-Fluoren-9-yl)methoxy)carbonyl)-2,2-dimethyloxazolidine-4-carboxylic acid is in asymmetric synthesis. By utilizing its chiral nature, chemists can introduce chirality into molecules during the synthesis process, leading to the production of enantiomerically pure compounds. This is crucial in the pharmaceutical industry, where the stereochemistry of a molecule can significantly impact its biological activity and pharmacological properties.Additionally, this compound can be utilized as a protecting group in peptide synthesis. The oxazolidine moiety can temporarily mask the amino group of amino acids, allowing selective reactions to occur on other functional groups without affecting the protected amine. This strategy is commonly employed in peptide chemistry to control the sequence and stereochemistry of peptide bonds.Overall, (S)-3-(((9H-Fluoren-9-yl)methoxy)carbonyl)-2,2-dimethyloxazolidine-4-carboxylic acid plays a vital role in the strategic design and synthesis of complex organic molecules, enabling chemists to access new and diverse chemical structures with precise control over stereochemistry.