- Description
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Details
(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-methylsulfanylbutanoic acid - Additional Information
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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
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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). - Reviews
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Peptides & Peptide Synthesis Products