N-[(tert-Butoxy)carbonyl]-L-tryptophan

Names

[ Name ]:
N-[(tert-Butoxy)carbonyl]-L-tryptophan

[Synonym ]:
N-(tert-Butoxycarbonyl)-L-tryptophan
EINECS 236-072-7
Boc-L-Trp
(S)-2-((tert-Butoxycarbonyl)amino)-3-(1H-indol-3-yl)propanoic acid
MFCD00065595
Boc-D-Trp-OH
N-tert-Butoxycarbonyl-L-tryptophan
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-tryptophan
Na-(tert-Butoxycarbonyl)-L-tryptophan
L-Tryptophan, N-[(1,1-dimethylethoxy)carbonyl]-
(2S)-3-(1H-indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
Nalpha-Boc-L-Tryptophane
N-Boc-L-tryptophan
Boc-Trp-OH
Boc-L-tryptophan

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
535.7±45.0 °C at 760 mmHg

[ Melting Point ]:
136 °C (dec.)(lit.)

[ Molecular Formula ]:
C₁₆H₂₀N₂O₄

[ Molecular Weight ]:
304.341

[ Flash Point ]:
277.8±28.7 °C

[ Exact Mass ]:
304.142303

[ PSA ]:
91.42000

[ LogP ]:
2.89

[ Vapour Pressure ]:
0.0±1.5 mmHg at 25°C

[ Index of Refraction ]:
1.602

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xn

[ Risk Phrases ]:
R20/21/22

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933990090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2933990090

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Oxidative modification of tryptophan residues exposed to peroxynitrite.

Biochem. Biophys. Res. Commun. 234(1) , 82-4, (1997)

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 peroxynitrit...

Abilities of some tryptophan and phenylalanine derivatives to inhibit gastric acid secretion.

Biochim. Biophys. Acta 845(2) , 158-62, (1985)

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 ...

Methods for determination of electrophoretic mobility and stability of complexes originating in solutions during the chiral discrimination process.

Electrophoresis 19(2) , 276-81, (1998)

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...