1009335-39-0 | (2R,4R)-Benzyl 4-hydroxy-2-(hydroxymethyl)pyrrolidine-1-carboxylate

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$43.00	$31.00
1g	95%	in stock	$70.00	$49.00
5g	95%	in stock	$262.00	$184.00

Description

• Catalog Number: AE28676
• Chemical Name: (2R,4R)-Benzyl 4-hydroxy-2-(hydroxymethyl)pyrrolidine-1-carboxylate
• CAS Number: 1009335-39-0
• Molecular Formula: C13H17NO4
• Molecular Weight: 251.2784
• MDL Number: MFCD18837818
• SMILES: OC[C@H]1C[C@H](CN1C(=O)OCc1ccccc1)O

Computed Properties

• Complexity: 278
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 2
• Heavy Atom Count: 18
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 4
• XLogP3: 0.5

Upstream Synthesis Route

The compound (2R,4R)-benzyl 4-hydroxy-2-(hydroxyMethyl)pyrrolidine-1-carboxylate plays a crucial role in chemical synthesis as a versatile building block in organic chemistry. Its unique molecular structure allows it to participate in various reactions, enabling the synthesis of complex molecules in a controlled and efficient manner.This compound can be used as a chiral auxiliary in asymmetric synthesis to control the stereochemistry of a reaction. By incorporating (2R,4R)-benzyl 4-hydroxy-2-(hydroxyMethyl)pyrrolidine-1-carboxylate into the substrate, chemists can direct the formation of specific enantiomers, leading to the production of optically pure compounds with high selectivity.Furthermore, (2R,4R)-benzyl 4-hydroxy-2-(hydroxyMethyl)pyrrolidine-1-carboxylate can serve as a protecting group for aldehydes or ketones during multi-step synthesis. This protection strategy helps to prevent unwanted side reactions or undesired functional group interconversions, allowing for the sequential modification of a molecule while preserving its core structure.Overall, the utility of (2R,4R)-benzyl 4-hydroxy-2-(hydroxyMethyl)pyrrolidine-1-carboxylate in chemical synthesis highlights its significance as a valuable tool for constructing intricate organic compounds with specific stereochemical properties and functional group manipulations.