Peptides & Peptide Synthesis Products

Boc-Met-OH

Boc-Met-OH
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$21.00
Boc-Met-OH, Catalog No: 48084
(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-methylsulfanylbutanoic acid, CAS: 2488-15-5, MW: 249.33, Formula: C10H19NO4S
Catalog No: 48084
(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-methylsulfanylbutanoic acid, CAS: 2488-15-5, MW: 249.33, Formula: C10H19NO4S
Description

Details

(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-methylsulfanylbutanoic acid
Additional Information

Additional Information

Catalog Number 48084
CAS 2488-15-5
M.W. 249.33
Formula C10H19NO4S
IUPAC Name (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-methylsulfanylbutanoic acid
Synonym No
Also Known As
  • (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-methylsulfanylbutanoic acid
  • (2S)-2-(tert-butoxycarbonylamino)-4-methylsulfanyl-butanoic acid
  • (2S)-2-[(tert-butoxy-oxomethyl)amino]-4-(methylthio)butanoic acid
  • (2S)-2-(tert-butoxycarbonylamino)-4-(methylthio)butyric acid
  • (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-methylsulfanyl-butanoic acid
  • Boc-Met-OH
  • N-(tert-Butoxycarbonyl)-L-methionine
  • Boc-L-methionine
  • 408425_ALDRICH
  • ST5307209
InChIKey IMUSLIHRIYOHEV-ZETCQYMHSA-N
InChI InChI=1S/C10H19NO4S/c1-10(2,3)15-9(14)11-7(8(12)13)5-6-16-4/h7H,5-6H2,1-4H3,(H,11,14)(H,12,13)/t7-/m0/s1
SMILES CC(C)(C)OC(=O)N[C@@H](CCSC)C(=O)O
Cited Uses

Details

1. Alam S et al, "Novel dipeptide nanoparticles for effective curcumin delivery", International Journal of Nanomedicine, 7() pp.4207-4222 (2012).
2. 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).
3. Boldt GE et al, "Synthesis, characterization and development of a high-throughput methodology for the discovery of botulinum neurotoxin A inhibitors", Journal of combinatorial chemistry, 8(4) pp.513-521 (2006).
4. Toida I et al, "Lack of tuberculin activity of synthetic peptides.", Infection and Immunity, 50(3) pp.614-619 (1985 Dec).
5. Kullmann W et al, "Protease-catalyzed peptide bond formation: application to synthesis of the COOH-terminal octapeptide of cholecystokinin.", Proceedings of the National Academy of Sciences of the United States of America, 79(9) pp.2840-2844 (1982 May).
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