Peptides & Peptide Synthesis Products

Boc-Tyr-OH

Boc-Tyr-OH

$11.00
$11.00
Boc-Tyr-OH, Catalog No: 48118
(2S)-3-(4-hydroxyphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid, CAS: 3978-80-1, MW: 281.30, Formula: C14H19NO5
Catalog No: 48118
(2S)-3-(4-hydroxyphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid, CAS: 3978-80-1, MW: 281.30, Formula: C14H19NO5
Description

Details

(2S)-3-(4-hydroxyphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
Additional Information

Additional Information

Catalog Number 48118
CAS 3978-80-1
M.W. 281.30
Formula C14H19NO5
IUPAC Name (2S)-3-(4-hydroxyphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
Synonym No
Also Known As
  • (2S)-3-(4-hydroxyphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
  • (2S)-2-(tert-butoxycarbonylamino)-3-(4-hydroxyphenyl)propanoic acid
  • (2S)-2-[(tert-butoxy-oxomethyl)amino]-3-(4-hydroxyphenyl)propanoic acid
  • (2S)-2-(tert-butoxycarbonylamino)-3-(4-hydroxyphenyl)propionic acid
  • N-(tert-Butoxycarbonyl)-L-tyrosine
  • 374229_ALDRICH
  • 15520_FLUKA
  • Boc-L-tyrosine
  • Boc-Tyr-OH
InChIKey CNBUSIJNWNXLQQ-NSHDSACASA-N
InChI InChI=1S/C14H19NO5/c1-14(2,3)20-13(19)15-11(12(17)18)8-9-4-6-10(16)7-5-9/h4-7,11,16H,8H2,1-3H3,(H,15,19)(H,17,18)/t11-/m0/s1
SMILES CC(C)(C)OC(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)O
Cited Uses

Details

1. Ramapanicker R et al, "Applications of Propargyl Esters of Amino Acids in Solution-Phase Peptide Synthesis", International Journal of Peptides, 2011() pp.854952 (2011).
2. Balboni G et al, "Role of 2?,6?-Dimethyl-L-Tyrosine (Dmt) in Some Opioid Lead Compounds", Bioorganic & medicinal chemistry, 18(16) pp.6024-6030 (2010 Aug 15).
3. Torino D et al, "Synthesis and evaluation of new endomorphin-2 analogues containing (Z)-?,?-didehydro-phenylalanine (?ZPhe) residues", Journal of medicinal chemistry, 53(11) pp.4550-4554 (2010 Jun 10).
4. Mahoney ME et al, "Synthesis of a Cyclic Pentapeptide Mimic of the Active Site His-Tyr Cofactor of Cytochrome c Oxidase", The Journal of organic chemistry, 74(21) pp.8212-8218 (2009 Nov 6).
5. Koley D et al, "Chemoselective Nitration of Phenols with tert-Butyl Nitrite in Solution and on Solid Support", Organic letters, 11(18) pp.4172-4175 (2009 Sep 17).
6. Torino D et al, "Synthesis and evaluation of new endomorphin analogues modified at the Pro2 residue", Bioorganic & medicinal chemistry letters, 19(15) pp.4115-4118 (2009 Aug 1).
7. Mollica A et al, "Synthesis of Stable and Potent δ/μ Opioid Peptides: Analogues of H-Tyr-c[D-Cys-Gly-Phe-D-Cys]-OH by Ring-Closing Metathesis", Journal of medicinal chemistry, 50(13) pp.3138-3142 (2007 Jun 28).
8. Shiotani K et al, "Synthesis of 3,6-bis[H-Tyr/H-Dmt-NH(CH2)m,n]-2(1H)pyrazinone derivatives: function of alkyl chain length on opioid activity", Bioorganic & medicinal chemistry letters, 16(22) pp.5793-5796 (2006 Nov 15).
9. Matsubayashi Y et al, "Phytosulfokine-?, a sulfated pentapeptide, stimulates the proliferation of rice cells by means of specific high- and low-affinity binding sites", Proceedings of the National Academy of Sciences of the United States of America, 94(24) pp.13357-13362 (1997 Nov 25).
10. Angliker H et al, "The synthesis of inhibitors for processing proteinases and their action on the Kex2 proteinase of yeast.", Biochemical Journal, 293(Pt 1) pp.75-81 (1993 Jul 1).
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