Fmoc-Tyr(tBu)-OH

CAS: 71989-38-3

Ref. 3D-FLY-1737-PI

Product Information

• Name: Fmoc-Tyr(tBu)-OH
• Synonyms: (2S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-[4-[(2-methylpropan-2-yl)oxy]phenyl]propanoic acid, (2S)-3-[4-(tert-Butoxy)phenyl]-2-([[(9H-fluoren-9-yl)methoxy]carbonyl]amino)propanoic acid, (S)-3-(4-tert-Butoxyphenyl)-2-[[[(9H-fluoren-9-yl)methoxy]carbonyl]amino]propionic acid, <span class="text-smallcaps">L</span>-Tyrosine, O-(1,1-dimethylethyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, Fmoc-L-Tyr(tBu)-OH, Fmoc-Tyr(But)-OH, Fmoc-Tyr(OtBu)-OH, N-(9-Fluorenyl Methoxy Carbonyl)-O-Tertbutyl-L-Tyrosine, N-alpha-(9-fluorenylmethyloxycarbonyl)-O-t-butyl-L-tyrosine, N-fmoc-O-T-butyl-L-tyrosine, NSC 334301, O-(1,1-Dimethylethyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-<span class="text-smallcaps">L</span>-tyrosine, O-tert-butyl-N-[(9H-fluoren-9-ylmethoxy)carbonyl]tyrosine, Tyr(tBu)

Description

Fmoc-Tyr(tBu)-OH is a building block for the synthesis of peptides. It is reacted with tert-butyl alcohol and hydrochloric acid to produce the corresponding Fmoc-protected tyrosine. The Fmoc group can be removed by treatment with dicyclohexylcarbodiimide and tert-butyl alcohol, followed by saponification in aqueous base. The morphologies of the resulting free amino acids are determined by their solubility in organic solvents such as chloroform or ethyl acetate, as well as in water.

Building Blocks:
Fmoc-Tyr(tBu)-OH
tert-Butanol
Hydrochloric Acid
Dicyclohexylcarbodiimide
Saponified
Morphologies

• Brand: Biosynth

Chemical properties

• Molecular weight: 459.53 g/mol
• Formula: C₂₈H₂₉NO₅
• Purity: Min. 98.0 Area-%