Peptides & Peptide Synthesis Products

Boc-Val-OH

Boc-Val-OH

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Boc-Val-OH, Catalog No: 48125
(2S)-3-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid, CAS: 13734-41-3, MW: 217.26, Formula: C10H19NO4
Catalog No: 48125
(2S)-3-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid, CAS: 13734-41-3, MW: 217.26, Formula: C10H19NO4
Description

Details

(2S)-3-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid
Additional Information

Additional Information

Catalog Number 48125
CAS 13734-41-3
M.W. 217.26
Formula C10H19NO4
IUPAC Name (2S)-3-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid
Synonym No
Also Known As
  • (2S)-3-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid
  • (2S)-2-(tert-butoxycarbonylamino)-3-methyl-butanoic acid
  • (2S)-2-[(tert-butoxy-oxomethyl)amino]-3-methylbutanoic acid
  • (2S)-2-(tert-butoxycarbonylamino)-3-methyl-butyric acid
  • 91602-34-5
  • N-((1,1-Dimethylethoxy)carbonyl)-L-valine
  • EINECS 237-307-6
  • L-Valine, N-((1,1-dimethylethoxy)carbonyl)-
  • ST5307217
  • N-((tert-Butoxy)carbonyl)-L-valine
  • NSC 197197
  • Valine, N-carboxy-, N-tert-butyl ester, L- (8CI)
  • 359726_ALDRICH
  • (S)-2-(Boc-amino)-3-methylbutyric acid
  • 15528_FLUKA
  • Boc-L-valine
  • Boc-Val-OH
  • N-(tert-Butoxycarbonyl)-L-valine
InChIKey SZXBQTSZISFIAO-ZETCQYMHSA-N
InChI InChI=1S/C10H19NO4/c1-6(2)7(8(12)13)11-9(14)15-10(3,4)5/h6-7H,1-5H3,(H,11,14)(H,12,13)/t7-/m0/s1
SMILES CC(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. 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).
3. Wilfert S et al, "Water-Soluble, Biocompatible Polyphosphazenes with Controllable and pH-Promoted Degradation Behavior", Journal of polymer science. Part A, Polymer chemistry, 52(2) pp.287-294 (2014 Jan 15).
4. Dai HX et al, "Pd(II)-Catalyzed Ortho- or Meta-C-H Olefination of Phenol Derivatives", Journal of the American Chemical Society, 135(20) pp.7567-7571 (2013 May 22).
5. 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).
6. van der Linden WA et al, "Discovery of a potent and highly β1 specific proteasome inhibitor from a focused library of urea-containing peptide vinyl sulfones and peptide epoxyketones", Organic & biomolecular chemistry, 10(1) pp.181-194 (2012 Jan 7).
7. Engle KM et al, "Ligand-Accelerated Cross-Coupling of C(sp2)-H Bonds with Arylboron Reagents", Journal of the American Chemical Society, 133(45) pp.18183-18193 (2011 Nov 16).
8. 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 ().
9. 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).
10. Engle KM et al, "Constructing Multiply Substituted Arenes Using Sequential Pd(II)-Catalyzed C-H Olefination", Angewandte Chemie (International Ed. in English), 49(35) pp.6169-6173 (2010 Aug 16).
11. 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).
12. 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).
13. Lynas J et al, "Peptidyl inverse esters of p-methoxybenzoic acid: a novel class of potent inactivator of the serine proteases.", Biochemical Journal, 325(Pt 3) pp.609-616 (1997 Aug 1).
14. 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).
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