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Fmoc-N-Me-Tyr(tBu)-OH

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Fmoc-N-Me-Tyr(tBu)-OH manufacturers

  • Fmoc-N-Me-Tyr(tBu)-OH
  • Fmoc-N-Me-Tyr(tBu)-OH pictures
  • $100.00
  • 2026-10-10
  • CAS:133373-24-7
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 1000 KG
Fmoc-N-Me-Tyr(tBu)-OH Basic information
Product Name:Fmoc-N-Me-Tyr(tBu)-OH
Synonyms:(S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(4-tert-butoxyphenyl)propanoic acid;O-(tert-Butyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-L-tyrosine;FMOC-N-METHYL-O-TERT-BUTYL-L-TYROSINE;N-FMoc-N-Methyl-O-tert-butyl-L-tyrosine;fMoc-N-Me-tyr(tbu)-oh;FMOC-N-ALPHA-METHYL-O-T-BUTYL-L-TYROSINE;FMOC-METYR(TBU)-OH;FMOC-N-METHYL-O-T-BUTYL-L-TYROSINE
CAS:133373-24-7
MF:C29H31NO5
MW:473.56
EINECS:
Product Categories:amino acids;Tyrosine [Tyr, Y];N-Methyl Amino Acids;Fmoc-Amino acid series
Mol File:133373-24-7.mol
Fmoc-N-Me-Tyr(tBu)-OH Structure
Fmoc-N-Me-Tyr(tBu)-OH Chemical Properties
Melting point 186-191°C
Boiling point 638.9±55.0 °C(Predicted)
density 1.208
storage temp. 2-8°C
form powder or crystals
pka2.98±0.10(Predicted)
AppearanceWhite to off-white Solid
Optical Rotation[α]22/D -49.0°, c = 0.5% in DMF
Major Applicationpeptide synthesis
InChIKeyWTLSDEYZKFJXFT-SANMLTNESA-N
SMILESC(O)(=O)[C@H](CC1=CC=C(OC(C)(C)C)C=C1)N(C(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O)C
CAS DataBase Reference133373-24-7(CAS DataBase Reference)
Safety Information
WGK Germany 3
HS Code 2924 29 70
HazardClass IRRITANT
Storage Class11 - Combustible Solids
MSDS Information
Fmoc-N-Me-Tyr(tBu)-OH Usage And Synthesis
Chemical PropertiesWhite powder
Usespeptide synthesis
General DescriptionFmoc-N-Me-Tyr(tBu)-OH is an Fmoc protected tyrosine derivative that is potentially useful for proteomics studies and solid phase peptide synthesis techniques. Tyrosine is a very important amino acid - one of the few amino acids which is phosphorylated to vary the physical properties of the peptides, and is a precursor for the formation of iodinated thyroid hormones. The Fmoc group is typically removed with a base such as pyridine - an orthogonal de-protection strategy to the acid labilie Boc group.
reaction suitabilityreaction type: Fmoc solid-phase peptide synthesis
Synthesis(9H-Fluoren-9-yl)methyl carbonochloridate could be used as the starting material to synthesize Fmoc-N-Me-Tyr(tBu)-OH.
Fmoc-N-Me-Tyr(tBu)-OH
Tag:Fmoc-N-Me-Tyr(tBu)-OH(133373-24-7) Related Product Information
Boc-MeTyr(Me)-OH dcha Fmoc-D-homoArg(Et)2-OH·HCl Fmoc-Lys(Pal-Glu-OtBu)-OH (R)-N-Fmoc-(3-Pyridyl)alanine N-[(9H-Fluoren-9-ylMethoxy)carbonyl]-4-[[[(4S)-hexahydro-2,6-dioxo-4-pyriMidinyl]carbonyl]aMino]-L-phenylalanine FMoc-N-Me-Trp(Trt)-OH Boc-N-Me-D-Tyr(Me)-OH.DCHA Fmoc-MeTyr(Bzl)-OH Fmoc-MeTrp(Boc)-OH Fmoc-MeTrp-OH (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(4-methoxyphenyl)propanoic acid Fmoc-D-MeTyr(Bzl)-OH (R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(4-(tert-butoxy)phenyl)propanoic acid O-tert-Butyl-L-tyrosine Fmoc-N-methyl-L-phenylalanine Fmoc-Tyr(tBu)-OH Fmoc-N-Me-Tyr(tBu)-OH (S)-Fmoc-meta-tyrosine O-tert-butyl ether