1025019-40-2 | (2R,3R,4S,5R,6R)-2-(Acetoxymethyl)-6-amino-4-(benzyloxy)tetrahydro-2h-pyran-3,5-diyl diacetate

Packsize	Purity	Availability	Price	Discounted Price
25mg		4 weeks	$594.00	$416.00
50mg		4 weeks	$598.00	$419.00
100mg		4 weeks	$697.00	$488.00
250mg		4 weeks	$1,215.00	$850.00
500mg		4 weeks	$2,018.00	$1,413.00

Description

• Catalog Number: AX06894
• Chemical Name: (2R,3R,4S,5R,6R)-2-(Acetoxymethyl)-6-amino-4-(benzyloxy)tetrahydro-2h-pyran-3,5-diyl diacetate
• CAS Number: 1025019-40-2
• Molecular Formula: C19H25NO8
• Molecular Weight: 395.4037
• MDL Number: MFCD31803746
• SMILES: CC(=O)OC[C@H]1O[C@@H](N)[C@@H]([C@H]([C@@H]1OC(=O)C)OCc1ccccc1)OC(=O)C

Upstream Synthesis Route

The compound (2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-amino-4-(benzyloxy)tetrahydro-2H-pyran-3,5-diyl diacetate, commonly referred to as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure containing both amino and acetate functional groups allows for a wide range of synthetic transformations and applications.In chemical synthesis, $name$ is often used as a key intermediate in the preparation of complex molecules such as natural products, pharmaceuticals, and advanced materials. The acetate groups can be selectively cleaved or modified to introduce additional functional groups, enabling further elaboration of the molecule through various chemical reactions.Furthermore, the presence of the amino group provides opportunities for selective derivatization, enabling the attachment of various substituents or linkers to tailor the properties of the final compound. This flexibility makes $name$ a valuable tool in the synthesis of diverse compounds with specific structures and functionalities tailored to meet the desired application requirements.Overall, the strategic incorporation of (2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-amino-4-(benzyloxy)tetrahydro-2H-pyran-3,5-diyl diacetate in chemical synthesis offers a versatile platform for accessing complex molecules and advancing the frontiers of organic chemistry.