1279038-32-2 | (2S,4R)-1-Boc-2-Hydroxymethyl-4-aminopyrrolidine hydrochloride

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	2 weeks	$196.00	$137.00
250mg	95%	2 weeks	$316.00	$222.00
1g	95%	2 weeks	$623.00	$436.00

Description

• Catalog Number: AA43283
• Chemical Name: (2S,4R)-1-Boc-2-Hydroxymethyl-4-aminopyrrolidine hydrochloride
• CAS Number: 1279038-32-2
• Molecular Formula: C10H21ClN2O3
• Molecular Weight: 252.7383
• MDL Number: MFCD11101172
• SMILES: OC[C@@H]1C[C@H](CN1C(=O)OC(C)(C)C)N.Cl

Computed Properties

• Complexity: 237
• Covalently-Bonded Unit Count: 2
• Defined Atom Stereocenter Count: 2
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 3

Upstream Synthesis Route

The compound (2S,4R)-1-Boc-2-Hydroxymethyl-4-aminopyrrolidine hydrochloride is a versatile building block commonly used in chemical synthesis. Its unique structure makes it a valuable reagent for the preparation of various complex molecules in the field of organic chemistry. One of the key applications of (2S,4R)-1-Boc-2-Hydroxymethyl-4-aminopyrrolidine hydrochloride is in the synthesis of pharmaceutical compounds. By incorporating this compound into the chemical synthesis process, chemists can introduce specific functional groups at precise locations within the target molecule. This enables the creation of new drugs or therapeutic agents with enhanced biological activity or improved pharmacokinetic properties.Additionally, (2S,4R)-1-Boc-2-Hydroxymethyl-4-aminopyrrolidine hydrochloride can be utilized in the preparation of chiral building blocks. Asymmetric synthesis using this compound allows for the production of enantiomerically pure molecules, which is crucial in the pharmaceutical industry where the biological activity of a drug often depends on its stereochemistry.Furthermore, this compound serves as a valuable intermediate in the synthesis of natural products, agrochemicals, and materials science. Its versatility and compatibility with a wide range of reaction conditions make it a preferred choice for chemists seeking to streamline their synthetic routes and achieve efficient transformations in their target molecule synthesis.