25616-33-5

Basic information

• Product Name: BOC-PHE-GLY-OH
• Synonyms: BOC-L-PHENYLALANINE GLYCINE;BOC-PHE-GLY-OH;Boc-Phe-Gly-OH≥ 99% (HPLC);(Tert-Butoxy)Carbonyl Phe-Gly-OH;Boc-Phe-Gly
• CAS NO: 25616-33-5
• Molecular Formula: C₁₆H₂₂N₂O₅
• Molecular Weight: 322.36
• Mol File: 25616-33-5.mol
• Article Data: 19

Chemical Properties

• Melting Point: 163-164 °C (decomp)
• Boiling Point: 588.5°C at 760 mmHg
• Flash Point: 309.7°C
• Appearance: /
• Density: 1.204g/cm³
• Vapor Pressure: 1.08E-14mmHg at 25°C
• Refractive Index: 1.535
• Storage Temp.: -15°C
• PKA: 3.41±0.10(Predicted)
• CAS DataBase Reference: BOC-PHE-GLY-OH(CAS DataBase Reference)
• NIST Chemistry Reference: BOC-PHE-GLY-OH(25616-33-5)
• EPA Substance Registry System: BOC-PHE-GLY-OH(25616-33-5)

Safety Data

• Hazard Codes: Xi
• Statements: 43
• Safety Statements: 36/37
• Hazardous Substances Data: 25616-33-5(Hazardous Substances Data)

Usage

Chemical Properties

White powder

InChI:InChI=1/C16H22N2O5/c1-16(2,3)23-15(22)18-12(14(21)17-10-13(19)20)9-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,17,21)(H,18,22)(H,19,20)

Upstream product

• 7625-57-2 methyl 2-((2S)-2-((tert-butoxycarbonyl)amino)-3-phenylpropanamido)acetate 
• 51987-73-6 (S)-2-tert-butoxycarbonylamino-3-phenyl-propionic acid methyl ester 
• 6000-44-8 sodium glycinate 
• 42280-29-5 [(S)-2-tert-butoxycarbonylamino-3-phenylpropanoylamino]acetic acid benzyl ester 
• 78569-23-0 3-(N-t-butoxycarbonyl-L-phenylalanyl)-1,3-thiazolidine-2-thione 
• 56-40-6 glycine 
• 158840-15-4 glycine allyl ester 
• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 50903-54-3 N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanine pentafluorophenyl ester 
• 63-91-2 L-phenylalanine 
• 24424-99-5 di-tert-butyl dicarbonate 

Downstream Products

• 17790-88-4 Boc-Phe-NHNHPh 
• 42280-29-5 [(S)-2-tert-butoxycarbonylamino-3-phenylpropanoylamino]acetic acid benzyl ester 
• 100571-97-9 Boc-Phe-Gly-D-NH-CH(CH₃)C₆H₅ 
• 113208-43-8 BOC-Phe-Gly-ACHPA-Ile N-<(4-amino-2-methyl-5-pyrimidinyl)methyl>amide 
• 112151-88-9 N-(tert-butyloxycarbonyl)-L-phenylalanylglycyl-L-valyl-4(S)-amino-3(S)-hydroxy-6-methylheptanoyl-L-alanyl-L-phenylalanine methyl ester 
• 112151-87-8 N-(tert-butyloxycarbonyl)-N^?-imid-<(benzyloxy)methyl>-L-phenylalanylglycyl-L-histidyl-4(S)-amino-3(S)-hydroxy-6-methylheptanoyl-L-alanyl-L-phenylalanine methyl ester 
• 42726-70-5 Boc-Phe-Gly-NH₂ 
• 100571-96-8 Boc-Phe-Gly-NH-CH₂C₆H₅ 
• 73148-98-8 Boc-Phe-Gly-Leu-Met-NH₂ 
• 236424-90-1 N-tert-butyloxycarbonyl-L-phenylalanyl-glycyl-L-leucine allyl ester 
• 219674-31-4 crotyl N-(tert-butyloxycarbonyl)-(S)-phenylalanylglycinate 
• 219674-28-9 2-methylallyl N-(tert-butyloxycarbonyl)-(S)-phenylalanylglycinate 
• 1396909-85-5 C₃₆H₃₆N₄O₈ 
• 219674-32-5 crotyl N-trifluoroacetyl-(S)-phenylalanylglycinate 

Relevant articles and documents

Synthesis, photophysical, photochemical, DNA cleavage/binding and cytotoxic properties of pyrene oxime ester conjugates

A new series of (E)-pyrene oxime ester conjugates of carboxylic acids including amino acids were synthesized by coupling with an environment sensitive fluorophore 1-acetylpyrene. (E)-Pyrene oxime esters exhibited strong fluorescence properties and interestingly their fluorescence properties were found to be highly sensitive to the surrounding environment. Direct irradiation of the (E)-pyrene oxime esters by UV light (≥350 nm) resulted in both the photo-Beckmann rearrangement product and products resulting from N-O bond homolysis. Photoproduct formation and their distribution were found to be solvent dependent. Further, we also showed (E)-pyrene oxime esters intercalated into DNA efficiently and photo-cleaved DNA. Finally we also showed these oxime esters can permeate cells efficiently and may cause cytotoxicity upon irradiation of light. The Royal Society of Chemistry and Owner Societies.

Influence of the dipeptide linker configuration on the activity of PSMA ligands

Selective ligands of an urea-based prostate specific membrane antigen with a phenylalanine/tyrosine-based dipeptide linker and with a mingled chiral centers configuration and/or substituted aromatic fragments were prepared in seven steps by liquid- and in

π-Stacking assisted redox active peptide-gallol conjugate: Synthesis of a new generation of low-toxicity antimicrobial silver nanoparticles

In this study, we describe the rational design and synthesis of a redox-active petide-gallol conjugate and explore its application in the preparation of antimicrobial silver nanoparticles. Increase in acidity and redox activity of peptide-gallol compounds