101469-92-5 | (S)-1-BOC-3-hydroxypyrrolidine

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$16.00	$11.00
5g	97%	in stock	$23.00	$16.00
25g	97%	in stock	$29.00	$20.00
100g	97%	in stock	$79.00	$55.00

Description

• Catalog Number: AB42945
• Chemical Name: (S)-1-BOC-3-hydroxypyrrolidine
• CAS Number: 101469-92-5
• Molecular Formula: C9H17NO3
• Molecular Weight: 187.2362
• MDL Number: MFCD01317839
• SMILES: O[C@H]1CCN(C1)C(=O)OC(C)(C)C

Computed Properties

• Complexity: 198
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2
• XLogP3: 0.6

Upstream Synthesis Route

$Name$ is a versatile compound that serves a crucial role in chemical synthesis, particularly in the field of organic chemistry. This compound, also known as (S)-1-(Tert-Butoxycarbonyl)-3-Hydroxypyrrolidine, is commonly utilized as a chiral building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals.Its unique structure and chirality make it an ideal starting material for the synthesis of complex molecules with specific stereochemical requirements. By incorporating (S)-1-(Tert-Butoxycarbonyl)-3-Hydroxypyrrolidine into synthetic routes, chemists can efficiently control the stereochemistry of the final product, leading to enhanced biological activity and improved efficiency.Furthermore, this compound's stability and compatibility with a wide range of reaction conditions make it a valuable tool for chemists working on the synthesis of intricate organic compounds. Its ability to undergo various functional group transformations and asymmetric reactions further highlights its utility in the development of novel molecules with potential therapeutic applications.Overall, (S)-1-(Tert-Butoxycarbonyl)-3-Hydroxypyrrolidine plays a vital role in enabling the efficient and precise synthesis of complex organic molecules, making it an indispensable component in modern chemical research and development.