1217786-73-6 | Boc-(R)-2-methoxy-phenylglycine

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$132.00	$93.00
250mg	98%	in stock	$218.00	$153.00
1g	98%	in stock	$309.00	$217.00

Description

• Catalog Number: AA54206
• Chemical Name: Boc-(R)-2-methoxy-phenylglycine
• CAS Number: 1217786-73-6
• Molecular Formula: C14H19NO5
• Molecular Weight: 281.30436000000003
• MDL Number: MFCD07371751
• SMILES: COc1ccccc1[C@H](C(=O)O)NC(=O)OC(C)(C)C

Computed Properties

• Complexity: 350
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 20
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 6
• XLogP3: 2.2

Upstream Synthesis Route

In chemical synthesis, (R)-2-((tert-Butoxycarbonyl)amino)-2-(2-methoxyphenyl)acetic acid serves as a crucial chiral building block for the creation of complex organic molecules. Its stereochemistry and functional groups make it a versatile compound that can be used in the production of pharmaceuticals, agrochemicals, and specialty chemicals. This compound is particularly valuable in asymmetric synthesis where precise control over the stereochemistry is essential for obtaining the desired product with high enantiomeric purity. Its presence can lead to the formation of new carbon-carbon or carbon-heteroatom bonds through a variety of reactions such as acylation, amidation, and Suzuki coupling, enabling the preparation of diverse molecular structures with specific biological or physical properties. Additionally, the (R)-2-((tert-Butoxycarbonyl)amino)-2-(2-methoxyphenyl)acetic acid can be used as a protecting group for amines, allowing for selective transformations in multi-step synthesis without affecting other functional groups. Its compatibility with various reaction conditions and compatibility with common reagents make it a valuable tool for synthetic chemists seeking to access challenging molecular targets in an efficient and sustainable manner.