1138324-46-5 | tert-Butyl (2s,4r)-2-(aminomethyl)-4-fluoro-1-pyrrolidinecarboxylate

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$192.00	$134.00
250mg	95%	in stock	$287.00	$201.00
500mg	95%	in stock	$430.00	$301.00
1g	95%	in stock	$731.00	$512.00
5g	95%	in stock	$2,499.00	$1,749.00

Description

• Catalog Number: AA12544
• Chemical Name: tert-Butyl (2s,4r)-2-(aminomethyl)-4-fluoro-1-pyrrolidinecarboxylate
• CAS Number: 1138324-46-5
• Molecular Formula: C10H19FN2O2
• Molecular Weight: 218.2685
• MDL Number: MFCD23106393
• SMILES: NC[C@@H]1C[C@H](CN1C(=O)OC(C)(C)C)F

Upstream Synthesis Route

The compound (2S,4R)-tert-Butyl 2-(aminomethyl)-4-fluoropyrrolidine-1-carboxylate, commonly referred to as $name$, is a valuable building block in chemical synthesis. Its unique structure contains a fluorine atom and an aminomethyl group, making it versatile for use in various synthetic pathways.One key application of $name$ in chemical synthesis is its role as a chiral auxiliary. Due to its chiral center at the 2S position and the 4R configuration, this compound can be utilized to introduce stereochemical control in reactions. By attaching $name$ to a reactive functional group, it can guide the formation of stereospecific products during transformations such as asymmetric reductions, aldol reactions, and ring closures.Additionally, the tert-butyl group enhances the stability and solubility of $name$, allowing for easier handling and manipulation in organic reactions. The presence of the fluorine atom further expands its reactivity profile, enabling selective fluorination reactions or acting as a directing group in complex synthesis routes.Overall, (2S,4R)-tert-Butyl 2-(aminomethyl)-4-fluoropyrrolidine-1-carboxylate serves as a valuable tool for chemists seeking to control stereochemistry, introduce fluorine functionality, or enhance the efficiency of chemical transformations in their synthetic endeavors.