1164-16-5 | Z-Tyr-OH

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$6.00	$4.00
5g	98%	in stock	$7.00	$5.00
10g	98%	in stock	$9.00	$6.00
25g	98%	in stock	$20.00	$14.00
100g	98%	in stock	$71.00	$50.00
500g	98%	in stock	$310.00	$217.00

Description

• Catalog Number: AA15883
• Chemical Name: Z-Tyr-OH
• CAS Number: 1164-16-5
• Molecular Formula: C17H17NO5
• Molecular Weight: 315.3206
• MDL Number: MFCD00191899
• SMILES: O=C(N[C@H](C(=O)O)Cc1ccc(cc1)O)OCc1ccccc1

Computed Properties

• Complexity: 386
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 23
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 7
• XLogP3: 1.7

Upstream Synthesis Route

N-Benzyloxycarbonyl-L-tyrosine is a versatile compound widely used in chemical synthesis for its ability to serve as a protected amino acid. Its application in peptide synthesis is particularly notable, where it acts as a key building block for constructing complex peptide chains. By incorporating N-Benzyloxycarbonyl-L-tyrosine into peptide sequences, chemists can selectively protect the tyrosine residue, allowing for sequential and controlled peptide bond formation. This compound plays a crucial role in the controlled synthesis of peptides with specific sequences and functionalities, making it an indispensable tool in the field of chemical synthesis.

Literature

• Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

  Bioorganic & medicinal chemistry letters 20101101

• Supramolecular control of polyplex dissociation and cell transfection: efficacy of amino groups and threading cyclodextrins in biocleavable polyrotaxanes.

  Journal of controlled release : official journal of the Controlled Release Society 20081021

• Screening and chromatographic assessing of a novel IgG biomimetic ligand.

  Biomedical chromatography : BMC 20061001

• Rapid binding of concanavalin A and maltose-polyrotaxane conjugates due to mobile motion of alpha-cyclodextrins threaded onto a poly(ethylene glycol).

  Bioconjugate chemistry 20050101

• Total synthesis of (-)-tuberostemonine.

  Journal of the American Chemical Society 20021218