120705-67-1 | (5R,6S)-6-[(1R)-1-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]ethyl]-7-oxo-3-[(2r)-tetrahydro-2-furanyl]-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid 2-propenyl ester

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$22.00	$15.00
1g	98%	in stock	$45.00	$31.00
5g	98%	in stock	$131.00	$92.00
25g	98%	in stock	$434.00	$304.00

Description

• Catalog Number: AD74149
• Chemical Name: (5R,6S)-6-[(1R)-1-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]ethyl]-7-oxo-3-[(2r)-tetrahydro-2-furanyl]-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid 2-propenyl ester
• CAS Number: 120705-67-1
• Molecular Formula: C21H33NO5SSi
• Molecular Weight: 439.6409
• MDL Number: MFCD09039289
• SMILES: C=CCOC(=O)C1=C(S[C@H]2N1C(=O)[C@@H]2[C@H](O[Si](C(C)(C)C)(C)C)C)[C@H]1CCCO1

Upstream Synthesis Route

The compound (5R,6S)-Allyl 6-((R)-1-((tert-butyldimethylsilyl)oxy)ethyl)-7-oxo-3-((R)-tetrahydrofuran-2-yl)-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate, also known as $name$, is a versatile building block in chemical synthesis. Its unique structure containing a bicyclic system with a tetrahydrofuran ring and a thia-azabicyclic core lends itself to a variety of reactions and transformations.One of the key applications of $name$ in chemical synthesis is as a key intermediate in the preparation of complex molecules and natural products. Its functional groups, including the allyl, ester, ketone, and silyl ether moieties, can undergo selective modifications to introduce various substituents or create new stereocenters.$name$ can be used in the construction of chiral scaffolds, especially in the synthesis of bioactive compounds or pharmaceutical intermediates. Due to its structural features, it can participate in a range of cycloaddition reactions, carbon-carbon bond formations, and functional group manipulations to access diverse chemical space.Overall, the strategic incorporation of $name$ in chemical synthesis allows for the efficient assembly of complex molecular structures with high stereoselectivity, making it a valuable tool for organic chemists in the preparation of target molecules with potential biological or therapeutic relevance.