112741-50-1 | tert-Butyl (2s,3r)-(+)-6-oxo-2,3-diphenyl-4-morpholinecarboxylate

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$44.00	$31.00
5g	95%	in stock	$118.00	$83.00
10g	95%	in stock	$211.00	$148.00
25g	95%	in stock	$449.00	$315.00
100g	95%	in stock	$1,319.00	$923.00

Description

• Catalog Number: AB42806
• Chemical Name: tert-Butyl (2s,3r)-(+)-6-oxo-2,3-diphenyl-4-morpholinecarboxylate
• CAS Number: 112741-50-1
• Molecular Formula: C21H23NO4
• Molecular Weight: 353.4116
• MDL Number: MFCD00074953
• SMILES: O=C1CN(C(=O)OC(C)(C)C)[C@@H]([C@@H](O1)c1ccccc1)c1ccccc1

Computed Properties

• Complexity: 501
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 2
• Heavy Atom Count: 26
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• XLogP3: 3.9

Upstream Synthesis Route

The experimental compound (2S,3R)-(+)-N-tert-Butoxycarbonyl-6-oxo-2,3-diphenylmorpholine is a valuable reagent in chemical synthesis, particularly in the field of organic chemistry. This compound plays a crucial role as a chiral building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique stereochemistry and functional groups make it a versatile tool for the creation of complex molecules with high levels of enantioselectivity.When utilized in chemical synthesis, (2S,3R)-(+)-N-tert-Butoxycarbonyl-6-oxo-2,3-diphenylmorpholine can act as a key intermediate in the construction of biologically active compounds. Its structural features allow for precise control over the stereochemistry of the final product, ensuring the desired properties and activities are achieved. This compound is often employed in reactions such as asymmetric transformations, stereoselective reductions, and ring-closing reactions to introduce chirality and enhance the overall efficiency of the synthetic process.Furthermore, the presence of the tert-butoxycarbonyl protecting group enhances the compound's stability and selectivity, enabling it to participate in multiple reaction steps without unwanted side reactions. This protection strategy also facilitates the isolation and purification of intermediates during the synthesis of complex molecules. Overall, the application of (2S,3R)-(+)-N-tert-Butoxycarbonyl-6-oxo-2,3-diphenylmorpholine in chemical synthesis enables chemists to access a diverse array of structurally intricate and biologically relevant compounds with high levels of control and efficiency.