ChemicalBook--->CAS DataBase List--->221243-01-2

221243-01-2

221243-01-2 Structure

221243-01-2 Structure
IdentificationBack Directory
[Name]

HOMO-L-TYROSINE HBR
[CAS]

221243-01-2
[Synonyms]

H-HTY-OH HBR
H-HTYR-OH HBR
H-HOTYR-OH HBR
HOMO-TYROSINE HBR
alpha-Homotyrosine
HOMO-L-TYROSINE HBR
H-TYR(NO CH2)-OH HBR
HOMO-TYROSINE HYDROBROMIDE
DL-Homotyrosine Hydrobromide
(S)-4-Hydroxy-homophenylalanine
L-HOMOTYROSINE HYDROBROMIDE SALT
(2S)-2-amino-4-(4-hydroxyphenyl)butanoic acid
[Molecular Formula]

C10H13NO3
[MDL Number]

MFCD03490505
[MOL File]

221243-01-2.mol
[Molecular Weight]

195.22
Chemical PropertiesBack Directory
[Melting point ]

217-220 °C
[Boiling point ]

397.0±37.0 °C(Predicted)
[density ]

1.281±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[form ]

Solid
[pka]

2.30±0.10(Predicted)
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Uses]

L-Homotyrosine is a tyrosine derivative that can be used for solid-phase peptide synthesis[1].
[Definition]

ChEBI: L-Homotyrosine is a non-proteinogenic alpha-amino acid.
[References]

[1] Bérubé C, et al. Convenient route to Fmoc-homotyrosine via metallaphotoredox catalysis and its use in the total synthesis of anabaenopeptin cyclic peptides. Org Biomol Chem. 2023 Nov 22;21(45):9011-9020. DOI:10.1039/d3ob01608k
Spectrum DetailBack Directory
[Spectrum Detail]

HOMO-L-TYROSINE HBR(221243-01-2)1HNMR
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