15512
Boc-Trp-OH
≥99.0% (TLC)
Synonym(s):
Nα-(tert-Butoxycarbonyl)-L-tryptophan, Nα-Boc-L-tryptophan
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About This Item
Empirical Formula (Hill Notation):
C16H20N2O4
CAS Number:
Molecular Weight:
304.34
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
236-072-7
MDL number:
Beilstein/REAXYS Number:
39677
Quality Level
assay
≥99.0% (TLC)
optical activity
[α]20/D −20±1°, c = 1% in DMF
reaction suitability
reaction type: Boc solid-phase peptide synthesis
mp
136 °C (dec.) (lit.)
application(s)
peptide synthesis
SMILES string
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-/m0/s1
InChI key
NFVNYBJCJGKVQK-ZDUSSCGKSA-N
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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)
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Peroxidase catalyzed nitration of tryptophan derivatives
Sala A, et al.
European Journal of Biochemistry, 271(13), 2841-2852 (2004)
Bailey T , et al. et al.
Science of Synthesis: Houben-Weyl Methods of Molecular Transformations, 21 (2014)
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 15512-25KG-R | 04061838125132 |
| 15512-4X2.5L-R | 04061838741929 |
| 15512-5L-R | 04061838118127 |
| 15512-6X1L-R | 04061838118134 |
| 15512-1L-R | 04061838741912 |
| 15512-2.5L-R | 04061838125125 |
| 15512-5G-F | 04061832641621 |