1217710-00-3 | Boc-(S)-2-methoxy-phenylglycine

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$50.00	$35.00
250mg	98%	in stock	$119.00	$84.00
1g	98%	in stock	$407.00	$285.00
5g	98%	in stock	$1,670.00	$1,169.00
10g	98%	in stock	$3,064.00	$2,145.00

Description

• Catalog Number: AA54130
• Chemical Name: Boc-(S)-2-methoxy-phenylglycine
• CAS Number: 1217710-00-3
• Molecular Formula: C14H19NO5
• Molecular Weight: 281.3044
• MDL Number: MFCD07371752
• 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

(S)-2-((tert-Butoxycarbonyl)amino)-2-(2-methoxyphenyl)acetic acid, also known as $name$, is a valuable building block in chemical synthesis processes. This compound is commonly utilized in the field of organic chemistry for its ability to act as a chiral auxiliary, enabling the asymmetric synthesis of a wide range of pharmaceuticals, agrochemicals, and other fine chemicals.Specifically, (S)-2-((tert-Butoxycarbonyl)amino)-2-(2-methoxyphenyl)acetic acid is often employed in the preparation of enantiomerically pure compounds by serving as a chiral template during various synthetic transformations. Its unique structure and stereochemistry allow for the control of molecular chirality, crucial in the production of biologically active molecules with specific pharmacological properties.Furthermore, this compound can be selectively deprotected under mild conditions to reveal the desired chiral functionality in the final product, making it a versatile and efficient tool for synthetic chemists. Its application in chemical synthesis extends to the creation of diverse molecular structures with high stereocontrol, contributing to the advancement of medicinal chemistry and other research areas.