53267-93-9 | Boc-Tyr(Me)-OH

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$8.00	$5.00
1g	97%	in stock	$13.00	$9.00
5g	97%	in stock	$19.00	$13.00
10g	97%	in stock	$28.00	$19.00
25g	97%	in stock	$41.00	$29.00
100g	97%	in stock	$161.00	$113.00

Description

• Catalog Number: AI51933
• Chemical Name: Boc-Tyr(Me)-OH
• CAS Number: 53267-93-9
• Molecular Formula: C15H21NO5
• Molecular Weight: 295.3309
• MDL Number: MFCD00065603
• SMILES: COc1ccc(cc1)CC(C(=O)O)NC(=O)OC(C)(C)C

Computed Properties

• Complexity: 356
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 21
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 7
• XLogP3: 1.8

Upstream Synthesis Route

Boc-Tyr(Me)-OH is a valuable reagent in chemical synthesis, particularly in peptide synthesis and drug development. This compound, also known as N-tert-butoxycarbonyl-L-tyrosine methyl ester, serves as a key building block for creating peptide molecules.One of the primary applications of Boc-Tyr(Me)-OH is as a protected amino acid. The Boc (tert-butoxycarbonyl) group acts as a temporary protective group for the amino function of tyrosine, allowing it to undergo specific chemical reactions without affecting other parts of the molecule. This selective protection and deprotection strategy is crucial in controlling the order of amino acid coupling in peptide synthesis.Additionally, the methyl ester group in Boc-Tyr(Me)-OH provides additional versatility in peptide assembly. The ester functionality can be easily manipulated through various chemical transformations, enabling the introduction of custom modifications or facilitating the attachment of other functional groups to the peptide backbone.In summary, Boc-Tyr(Me)-OH plays a significant role in the precise and controlled construction of peptides, making it a valuable tool for chemists engaged in the synthesis of complex biomolecules and pharmaceuticals.