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Documenti

15185

Sigma-Aldrich

Boc-D-Trp-OH

≥98.0% (TLC)

Sinonimo/i:

Nα-Boc-D-tryptophan

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About This Item

Formula empirica (notazione di Hill):
C16H20N2O4
Numero CAS:
Peso molecolare:
304.34
Beilstein:
4237334
Numero CE:
Numero MDL:
Codice UNSPSC:
12352209
eCl@ss:
32160406
ID PubChem:
NACRES:
NA.22

Saggio

≥98.0% (TLC)

Impiego in reazioni chimiche

reaction type: Boc solid-phase peptide synthesis

applicazioni

peptide synthesis

Stringa SMILE

CC(C)(C)OC(=O)N[C@H](Cc1c[nH]c2ccccc12)C(O)=O

InChI

1S/C16H20N2O4/c1-16(2,3)22-15(21)18-13(14(19)20)8-10-9-17-12-7-5-4-6-11(10)12/h4-7,9,13,17H,8H2,1-3H3,(H,18,21)(H,19,20)/t13-/m1/s1
NFVNYBJCJGKVQK-CYBMUJFWSA-N

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)


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R Vespalec et al.
Electrophoresis, 19(2), 276-281 (1998-04-21)
An equation for the calculation of electrophoretic mobility of kinetically labile complexes originating in solutions during the chiral discrimination process is derived. The mobility of the complex is calculated from that of a fully ionized racemic compound, measured in absence
Y Kato et al.
Biochemical and biophysical research communications, 234(1), 82-84 (1997-05-08)
The aim of this study was to clarify the mechanism of loss of Trp residues in proteins exposed to peroxynitrite. The Trp residues in bovine serum albumin and collagen IV were decreased by peroxynitrite treatment. To identify the degradation products
R Magous et al.
Biochimica et biophysica acta, 845(2), 158-162 (1985-05-30)
Benzotript (N-p-chlorobenzoyl-L-tryptophan) has been shown to be a receptor-antagonist in vivo and in vitro for peptides from the gastrin family. In the present study, we examine tryptophan, and some of its N- and C-acylated derivatives, as well as some phenylalanine
Denisa Folprechtová et al.
Electrophoresis, 40(15), 1972-1977 (2019-01-24)
Three chiral stationary phases were prepared by dynamic coating of sulfobutylether-β-cyclodextrin (SBE-β-CD) with different degrees of substitution, onto strong anion-exchange stationary phases. The enantioselective potential and stability of newly prepared chiral stationary phases were examined using a set of structurally

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