Peptides & Peptide Synthesis Products

Boc-Ala-OH

Boc-Ala-OH

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Boc-Ala-OH, Catalog No: 48001
(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid, CAS: 15761-38-3, MW: 189.21, Formula: C8H15NO4
Catalog No: 48001
(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid, CAS: 15761-38-3, MW: 189.21, Formula: C8H15NO4
Description

Details

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

Additional Information

Catalog Number 48001
CAS 15761-38-3
M.W. 189.21
Formula C8H15NO4
IUPAC Name (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
Synonym No
Also Known As
  • (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
  • (2S)-2-(tert-butoxycarbonylamino)propanoic acid
  • (2S)-2-[(tert-butoxy-oxomethyl)amino]propanoic acid
  • (2S)-2-(tert-butoxycarbonylamino)propionic acid
  • 186665-28-1
  • 207305-56-4
  • 90580-61-3
  • EINECS 239-847-8
  • L-Alanine, N-((1,1-dimethylethoxy)carbonyl)-
  • N-((1,1-Dimethylethoxy)carbonyl)-L-alanine
  • 15380_FLUKA
  • 134511_ALDRICH
  • Boc-Ala-OH
  • Boc-L-alanine
  • N-(tert-Butoxycarbonyl)-L-alanine
  • SBB016767
  • 492884_ALDRICH
  • Boc-Ala-OH-12C3
  • L-Alanine-12C3, N-t-Boc derivative
  • N-(tert-Butoxycarbonyl)-L-alanine-12C3
InChIKey QVHJQCGUWFKTSE-YFKPBYRVSA-N
InChI InChI=1S/C8H15NO4/c1-5(6(10)11)9-7(12)13-8(2,3)4/h5H,1-4H3,(H,9,12)(H,10,11)/t5-/m0/s1
SMILES C[C@@H](C(=O)O)NC(=O)OC(C)(C)C
Cited Uses

Details

1. Wong CT et al, "Realizing serine/threonine ligation: scope and limitations and mechanistic implication thereof", Frontiers in Chemistry, 2() pp.28 ().
2. Su Z et al, "ChIP-less analysis of chromatin states", Epigenetics & Chromatin, 7() pp.7 ().
3. Zeglis BM et al, "Building Blocks for the Construction of Bioorthogonally Reactive Peptides via Solid-Phase Peptide Synthesis", ChemistryOpen, 3(2) pp.48-53 (2014 Apr).
4. Cheng XF et al, "Pd(II)-Catalyzed Enantioselective C-H Activation/C-O Bond Formation: Synthesis of Chiral Benzofuranones", Journal of the American Chemical Society, 135(4) pp.1236-1239 (2013 Jan 30).
5. Stolze SC et al, "The Antimalarial Natural Product Symplostatin 4 Is a Nanomolar Inhibitor of the Food Vacuole Falcipains", Chemistry & biology, 19(12) pp.1546-1555 (2012 Dec 21).
6. Wu X et al, "Inhibition of Ras-Effector Interaction by Cyclic Peptides", MedChemComm, 4(2) pp.378-382 (2013 Feb 1).
7. Parrish AR et al, "Expanding the Genetic Code of Caenorhabditis elegans Using Bacterial aminoacyl-tRNA Synthetase/tRNA Pairs", ACS Chemical Biology, 7(7) pp.1292-1302 (2012 Jul 20).
8. Khoo KK et al, "Lactam-stabilized helical analogues of the analgesic ?-conotoxin KIIIA", Journal of medicinal chemistry, 54(21) pp.7558-7566 (2011 Nov 10).
9. Dong S et al, "Toward Homogeneous Erythropoietin: Application of Metal Free Dethiylation in the Chemical Synthesis of the Ala79-Arg166 Glycopeptide Domain", Israel journal of chemistry, 51(8-9) pp.968-976 (2011 Nov).
10. Matsuura K et al, "Syntheses and Self-assembling Behaviors of Pentagonal Conjugates of Tryptophane Zipper-Forming Peptide", International Journal of Molecular Sciences, 12(8) pp.5187-5199 ().
11. Ramapanicker R et al, "Applications of Propargyl Esters of Amino Acids in Solution-Phase Peptide Synthesis", International Journal of Peptides, 2011() pp.854952 (2011).
12. Crawford MJ et al, "Effect of Steric Constraint at the γ-Backbone Position on the Conformations and Hybridization Properties of PNAs", Journal of Nucleic Acids, 2011() pp.652702 ().
13. Engle KM et al, "Ligand-Accelerated C-H Activation Reactions: Evidence for a Switch of Mechanism", Journal of the American Chemical Society, 132(40) pp.14137-14151 (2010 Oct 13).
14. Lu Y et al, "Pd(II)-Catalyzed Hydroxyl-Directed C-H Olefination Enabled by Mono-Protected Amino Acid Ligands", Journal of the American Chemical Society, 132(16) pp.5916-5921 (2010 Apr 28).
15. Shi BF et al, "Pd(II)-Catalyzed Enantioselective C-H Olefination of Diphenylacetic Acids", Journal of the American Chemical Society, 132(2) pp.460-461 (2010 Jan 20).
16. Dutot L et al, "Glycosylated cell-penetrating peptides and their conjugates to a proapoptotic peptide: preparation by click chemistry and cell viability studies", Journal of Chemical Biology, 3(2) pp.51-65 ().
17. 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).
18. Sabidó E et al, "Activity-based probes for monitoring post-proline protease activity", Chembiochem : a European journal of chemical biology, 10(14) pp.2361-2366 (2009 Sep 21).
19. Foley D et al, "Targeting ketone drugs towards transport by the intestinal peptide transporter, PepT1 †Electronic supplementary information (ESI) available: Full experimental details for the synthesis, characterisation, testing and analysis of 16, with characterisation data for 17. See DOI: 10.1039/b818606e Click here for additional data file.", Organic & Biomolecular Chemistry, 7(6) pp.1064-1067 (2009 Mar 21).
20. Bibbs L et al, "Strategies for the synthesis of labeled peptides", Journal of Biomolecular Techniques : JBT, 11(4) pp.155-165 (2000 Dec).
21. Shrimpton CN et al, "Development and characterization of novel potent and stable inhibitors of endopeptidase EC 3.4.24.15.", Biochemical Journal, 345(Pt 2) pp.351-356 (2000 Jan 15).
22. Qi Z et al, "Structure-function study on a de novo synthetic hydrophobic ion channel.", Biophysical Journal, 76(2) pp.631-641 (1999 Feb).
23. Abiko T et al, "Syntheses of two deacetyl-thymosin ?1 analogues and their effects on low E-rosette-forming lymphocytes of uraemic patients", Mediators of Inflammation, 5(4) pp.295-298 (1996 Sep).
24. Irvine GB et al, "The kinetics of hydrolysis of some synthetic substrates containing neutral hydrophilic groups by pig pepsin and chicken liver cathepsin D.", Biochemical Journal, 211(1) pp.237-242 (1983 Apr 1).
25. Pierzchala PA et al, "A new fluorogenic substrate for plasmin.", Biochemical Journal, 183(3) pp.555-559 (1979 Dec 1).
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