92264-95-4

Basic information

• Product Name: N-(tert-butoxycarbonyl)-L-tyrosyl p-nitrobenzyl ester
• Synonyms: N-(tert-butoxycarbonyl)-L-tyrosyl p-nitrobenzyl ester
• CAS NO: 92264-95-4
• Molecular Weight: 416.431
• Mol File: 92264-95-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(tert-butoxycarbonyl)-L-tyrosyl p-nitrobenzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: N-(tert-butoxycarbonyl)-L-tyrosyl p-nitrobenzyl ester(92264-95-4)
• EPA Substance Registry System: N-(tert-butoxycarbonyl)-L-tyrosyl p-nitrobenzyl ester(92264-95-4)

Safety Data

• Hazardous Substances Data: 92264-95-4(Hazardous Substances Data)

Upstream product

• 3978-80-1 Boc-Tyr-OH 
• 100-11-8 1-bromomethyl-4-nitro-benzene 

Downstream Products

• 92265-00-4 (S)-N^α-(tert-butoxycarbonyl)-O-(O',O''-diethylphosphoro)-L-tyrosine 
• 118920-14-2 Boc-Tyr(PO₃Bzl₂)-Leu-Gly-OBzl 
• 118892-04-9 H-Tyr(PO₃H₂)-Leu-Gly-OH*TFA 
• 92265-01-5 N^α-(tert-butoxycarbonyl)-O-(O',O''-dibenzylphosphoro)-L-tyrosine 
• 443307-29-7 (S)-3-{4-[[(2S,3S,5R)-3-Azido-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethoxy]-(2-cyano-ethoxy)-phosphanyloxy]-phenyl}-2-tert-butoxycarbonylamino-propionic acid 4-nitro-benzyl ester 
• 443307-30-0 2-tert-butoxycarbonylamino-3-{4-[(2-cyano-ethoxy)-diisopropylamino-phosphanyloxy]-phenyl}-propionic acid 4-nitro-benzyl ester 
• 92264-96-5 N-(tert-Butoxycarbonyl)-O-(dimethylphosphono)-L-tyrosyl p-nitrobenzyl ester 
• 92264-97-6 (S)-2-tert-Butoxycarbonylamino-3-[4-(diethoxy-phosphoryloxy)-phenyl]-propionic acid 4-nitro-benzyl ester 
• 92264-98-7 N-(tert-butoxycarbonyl)-O-(dibenzylphosphono)-L-tyrosyl p-nitro-benzyl ester 
• 92264-99-8 N^α-(tert-butoxycarbonyl)-O-(O',O''-dimethylphosphoro)-L-tyrosine 

Relevant articles and documents

Synthesis of prodrug candidates: conjugates of amino acid with nucleoside boranophosphate.

[structure: see text] Preparation of antiviral and anticancer prodrug candidates, P-tyrosinyl(P-O)-5'-P-nucleosidyl boranophosphates, is described. One-pot synthesis via a phosphoramidite method resulted in the title compounds with good yields. The P-boranophosphate diastereomers were separated by RP-HPLC, and their structures were confirmed by 1H and 31P NMR spectroscopy and MS analysis.

Liquid Secondary Ionization Mass Spectrometric Characterization of Two Synthetic Phosphotyrosine-Containing Peptides

N-(tert-Butoxycarbonyl)-Q-(dibenzylphosphono)-L-tyrosine (1), a suitably protected phosphotyrosine, has been prepared for peptide synthesis.Compound 1 and its intermediate precursors were characterized by elemental analyses, liquid secondary ion mass spec