102195-80-2 | N-Boc-4-oxo-L-Proline methyl ester

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$6.00	$4.00
1g	98%	in stock	$8.00	$5.00
5g	98%	in stock	$8.00	$6.00
10g	98%	in stock	$12.00	$9.00
25g	98%	in stock	$18.00	$13.00
100g	98%	in stock	$57.00	$40.00
500g	98%	in stock	$284.00	$199.00

Description

• Catalog Number: AA08708
• Chemical Name: N-Boc-4-oxo-L-Proline methyl ester
• CAS Number: 102195-80-2
• Molecular Formula: C11H17NO5
• Molecular Weight: 243.2564
• MDL Number: MFCD01861778
• SMILES: COC(=O)[C@@H]1CC(=O)CN1C(=O)OC(C)(C)C

Computed Properties

• Complexity: 344
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 17
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• XLogP3: 0.6

Upstream Synthesis Route

(S)-tert-Butyl 2-(methoxycarbonyl)-4-oxopyrrolidine-1-carboxylate is a versatile compound widely utilized in chemical synthesis. Its chiral nature and unique structural features make it a valuable building block for the preparation of various molecules in the field of organic chemistry. This compound plays a crucial role in asymmetric synthesis, allowing for the creation of enantiomerically pure compounds. By serving as a chiral auxiliary or a key intermediate, (S)-tert-Butyl 2-(methoxycarbonyl)-4-oxopyrrolidine-1-carboxylate enables the controlled formation of stereocenters in complex molecules. Its presence can dictate the stereochemistry of subsequent reactions, leading to the desired enantiomer selectivity.Furthermore, (S)-tert-Butyl 2-(methoxycarbonyl)-4-oxopyrrolidine-1-carboxylate can participate in various transformations such as nucleophilic additions, ring-closing reactions, and functional group manipulations. Its reactivity and stability under typical synthetic conditions make it a reliable reagent for the construction of diverse chemical structures.In summary, the application of (S)-tert-Butyl 2-(methoxycarbonyl)-4-oxopyrrolidine-1-carboxylate in chemical synthesis offers chemists a powerful tool for the efficient and controlled preparation of enantiomerically pure compounds with tailored stereochemistry.