Boc-Tyr-OH

Modify Date: 2024-01-02 18:03:13

Boc-Tyr-OH Structure
Boc-Tyr-OH structure
 Common Name Boc-Tyr-OH
CAS Number 3978-80-1 Molecular Weight 281.304
Density 1.2±0.1 g/cm3 Boiling Point 484.9±40.0 °C at 760 mmHg
Molecular Formula C14H19NO5 Melting Point 135-140ºC
MSDS Chinese USA Flash Point 247.1±27.3 °C

 Use of Boc-Tyr-OH


(S)-2-((tert-Butoxycarbonyl)amino)-3-(4-hydroxyphenyl)propanoic acid is a tyrosine derivative[1].

 Names

Name (2S)-3-(4-hydroxyphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate
Synonym More Synonyms

 Boc-Tyr-OH Biological Activity

Description (S)-2-((tert-Butoxycarbonyl)amino)-3-(4-hydroxyphenyl)propanoic acid is a tyrosine derivative[1].
Related Catalog
In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

 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

 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

 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%

 Articles3

More Articles
Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

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 ...

 Synonyms

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
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