Boc-Tyr-OH
Names
[ CAS No. ]:
3978-80-1
[ Name ]:
Boc-Tyr-OH
[Synonym ]:
N-tert-butoxycarbonyl-L-tyrosine
N-t-butoxycarbonyl-L-tyrosine
L-Tyrosine, N-[(1,1-dimethylethoxy)carbonyl]-
Boc-L-tryptophan
Boc-L-Trp-OH
MFCD00037179
Boc-Tyr-OH
Boc-Trp-OH
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-tyrosine
BOC-L-Tyrosine
N-((tert-Butoxy)carbonyl)-L-tyrosine
N-Boc-L-tyrosine
N-Boc-L-tryptophan
EINECS 223-613-7
N-(tert-Butoxycarbonyl)-L-tyrosine
Biological Activity
[Description]:
[Related Catalog]:
[In Vitro]
[References]
Chemical & Physical Properties
[ Density]:
1.2±0.1 g/cm3
[ Boiling Point ]:
484.9±40.0 °C at 760 mmHg
[ Melting Point ]:
135-140ºC
[ Molecular Formula ]:
C14H19NO5
[ Molecular Weight ]:
281.304
[ Flash Point ]:
247.1±27.3 °C
[ Exact Mass ]:
281.126312
[ PSA ]:
95.86000
[ LogP ]:
2.23
[ Vapour Pressure ]:
0.0±1.3 mmHg at 25°C
[ Index of Refraction ]:
1.550
MSDS
Safety Information
[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
[ Hazard Codes ]:
Xi
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S24/25
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2924299090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2924299090
[ Summary ]:
2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
Articles
Nat. Chem. Biol. 5 , 45-52, (2009)
Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting tr...
Analyte separation by OMNiMIPs imprinted with multiple templates.Biosens. Bioelectron. 25(3) , 604-8, (2009)
Changes detected in the imprinting effect by OMNiMIPs imprinted with multiple templates appear to be a function of the maximum template loading. Below the maximum template loading, the polymers imprin...
Tyrosine derivatization and preparative purification of the sialyl and asialy-N-linked oligosaccharides from porcine fibrinogen.Arch. Biochem. Biophys. 312(1) , 151-7, (1994)
The N-linked oligosaccharides from porcine fibrinogen were purified following their release from glycopeptides using N-glycosidase F. In separate experiments, both sialyl and asialyl oligosaccharides ...