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Merck
CN

15185

Boc-D-Trp-OH

≥98.0% (TLC)

Synonym(s):

Nα-Boc-D-tryptophan

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About This Item

Empirical Formula (Hill Notation):
C16H20N2O4
CAS Number:
5241-64-5
Molecular Weight:
304.34
NACRES:
NA.22
PubChem Substance ID:
57647336
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
226-042-1
MDL number:
MFCD00037944
Beilstein/REAXYS Number:
4237334

Key Documents

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InChI key

NFVNYBJCJGKVQK-CYBMUJFWSA-N

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

SMILES string

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

assay

≥98.0% (TLC)

reaction suitability

reaction type: Boc solid-phase peptide synthesis

application(s)

peptide synthesis

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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCCH9165
BCBQ9170V
BCBM1786V
BCBJ0993V
1402456V

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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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