Peptides & Peptide Synthesis Products

Boc-Gln-OH

Boc-Gln-OH

$15.00
$15.00
Boc-Gln-OH, Catalog No: 48041
(2S)-5-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxopentanoic acid, CAS: 13726-85-7, MW: 246.26, Formula: C10H18N2O5
Catalog No: 48041
(2S)-5-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxopentanoic acid, CAS: 13726-85-7, MW: 246.26, Formula: C10H18N2O5
Description

Details

(2S)-5-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxopentanoic acid
Additional Information

Additional Information

Catalog Number 48041
CAS 13726-85-7
M.W. 246.26
Formula C10H18N2O5
IUPAC Name (2S)-5-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxopentanoic acid
Synonym No
Also Known As
  • (2S)-5-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxopentanoic acid
  • (2S)-5-amino-2-(tert-butoxycarbonylamino)-5-oxo-pentanoic acid
  • (2S)-5-amino-2-[(tert-butoxy-oxomethyl)amino]-5-oxopentanoic acid
  • (2S)-5-amino-2-(tert-butoxycarbonylamino)-5-keto-valeric acid
  • (2S)-5-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxo-pentanoic acid
  • 2483-14-9
  • N2-((1,1-Dimethylethoxy)carbonyl)-L-glutamine
  • 408441_ALDRICH
  • Boc-Gln-OH
  • Boc-L-glutamine
  • Nalpha-(tert-Butoxycarbonyl)-L-glutamine
  • EINECS 237-296-8
  • Glutamine, N2-carboxy-, N2-tert-butyl ester, L- (8CI)
  • L-Glutamine, N2-((1,1-dimethylethoxy)carbonyl)-
  • ST5307203
  • tert-Butoxycarbonyl-L-glutamine
  • N2-((tert-Butoxy)carbonyl)-L-glutamine
  • NSC 334370
  • Nalpha-tert-Butoxycarbonyl-L-glutamine
  • N(alpha)-tert-Butoxycarbonyl-L-glutamine
InChIKey VVNYDCGZZSTUBC-LURJTMIESA-N
InChI InChI=1S/C10H18N2O5/c1-10(2,3)17-9(16)12-6(8(14)15)4-5-7(11)13/h6H,4-5H2,1-3H3,(H2,11,13)(H,12,16)(H,14,15)/t6-/m0/s1
SMILES CC(C)(C)OC(=O)N[C@@H](CCC(=O)N)C(=O)O
Cited Uses

Details

1. Hingorani DV et al, "A catalyCEST MRI contrast agent that detects the enzyme-catalyzed creation of a covalent bond", Journal of the American Chemical Society, 135(17) pp.6396-6398 (2013 May 1).
2. Wu X et al, "A novel high-yield synthesis of aminoacyl p-nitroanilines and aminoacyl 7-amino-4-methylcoumarins: Important synthons for the synthesis of chromogenic/fluorogenic protease substrates", Beilstein Journal of Organic Chemistry, 7() pp.1030-1035 ().
3. You L et al, "Anion transport properties of amine and amide-sidechained peptides are affected by charge and phospholipid composition", Organic & biomolecular chemistry, 6(16) pp.2914-2923 (2008 Aug 21).
4. Toida I et al, "Lack of tuberculin activity of synthetic peptides.", Infection and Immunity, 50(3) pp.614-619 (1985 Dec).
5. Yamashiro D et al, "Synthesis and biological activity of human inhibin-like peptide-(1-31).", Proceedings of the National Academy of Sciences of the United States of America, 81(17) pp.5399-5402 (1984 Sep).
6. Andreu D et al, "Solid-phase synthesis of cecropin A and related peptides.", Proceedings of the National Academy of Sciences of the United States of America, 80(21) pp.6475-6479 (1983 Nov).
7. Li CH et al, "Total synthesis of insulin-like growth factor I (somatomedin C).", Proceedings of the National Academy of Sciences of the United States of America, 80(8) pp.2216-2220 (1983 Apr).
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