80971-82-0

Usage

Uses

Used in Peptide Synthesis:
BOC-TYR(AC)-OH is used as a building block in the solid-phase peptide synthesis process for the creation of specific peptide sequences. Its protecting groups allow for controlled manipulation and deprotection during peptide assembly, ensuring the accurate formation of desired peptide structures.
Used in Research and Development:
BOC-TYR(AC)-OH is used as a reagent in the development of custom peptides for research purposes, enabling scientists to explore the properties and potential applications of novel peptide sequences.
Used in Drug Development:
In the pharmaceutical industry, BOC-TYR(AC)-OH is utilized for the synthesis of peptides with therapeutic potential, contributing to the discovery and development of new drugs and treatments.
Used in Biochemistry and Molecular Biology:
BOC-TYR(AC)-OH is employed in various applications within biochemistry and molecular biology, such as the study of protein structure and function, as well as the development of diagnostic tools and therapeutic agents based on peptide sequences.

Upstream product

• 3978-80-1 Boc-Tyr-OH 
• 108-24-7 acetic anhydride 

Downstream Products

• 291313-44-5 (S)-N-[(S)-1-benzyl-2-hydroxyethyl]-3-(4-acetoxyphenyl)-2-[N-(tert.butoxycarbonyl)amino]propionamide 
• 18938-60-8 (S)-tert-butyl 2-((tert-butoxycarbonyl)amino)-3-(4-hydroxyphenyl)propanoate 
• 1188307-55-2 Boc-Tyr(Ac)-Gly-Gly-OAll 
• 142978-59-4 Acetic acid 4-((S)-2-{4-[3-(3-amino-propylamino)-propylamino]-butylcarbamoyl}-2-butyrylamino-ethyl)-phenyl ester 
• 474070-52-5 N-butyryl-O-acetyl-L-tyrosine p-nitrophenyl ester 
• 80971-85-3 (S)-2-{(S)-2-[2-({1-[(S)-3-(4-Acetoxy-phenyl)-2-amino-propionylamino]-cyclopropanecarbonyl}-amino)-acetylamino]-3-phenyl-propionylamino}-4-methyl-pentanoic acid 
• 80971-87-5 1-(L-tyrosyl)aminocyclopropane-1-carbonylglycyl-L-phenylalanyl-L-leucine 
• 291313-54-7 (S)-2-[(S)-2-(4-acetoxyphenyl)-1-[N-(tert-butoxycarbonyl)amino]ethyl]-4-benzyl-2-oxazoline 
• 210707-19-0 (S)-4-benzyl-2-[(S)-1-[N-(tert-butoxycarbonyl)amino]-2-(4-hydroxyphenyl)ethyl]-2-oxazoline 

Relevant academic research and scientific papers

Synergistic Photobactericidal Activity Based on Ultraviolet-A Irradiation and Ferulic Acid Derivatives

Ultraviolet-A (UV-A)-mediated bactericidal activity was enhanced by combined treatment with trans-ferulic acid (trans-FA, compound 1) or its derivatives. Derivative compounds 4 and 10 contain a phenyl group or an l-tyrosine HCl tert-butyl ester, respectiv

New oxidative transformations of phenolic and indolic oxazolines: An avenue to useful azaspirocyclic building-blocks

The oxidative cyclization of a phenolic amide to a spirolactam has long been regarded as an 'impossible' reaction, because exposure of the substrates to a variety of oxidants results in formation of spirolactones with consequent loss of the amine segment. We recently communicated that this heretofore unknown transformation may be achieved by oxidation of oxazoline analogues of phenolic and indolic amides. Herein, we provide full details of our work.

Synthesis of spirolactams from tyrosine amides and related substances

Oxidation of oxazolines derived from phenolic ω-arylalkanoic acids such as tyrosine with iodobenzene diacetate leads to spirocyclic amides in moderate yields. This reaction was heretofore unknown due to the propensity of free amide analogs of the oxazolin

Peptide Synthesis with 1-Aminocyclopropane-1-carboxylic Acid

Peptide derivatives of 1-aminocyclopropane-1-carboxylic acid have been synthesized by model active ester coupling reactions in order to compare the steric effect of this plant amino acid with that of its open-chain congener 2-methylalanine.An analogue of