Z-D-Phe-OH

Modify Date: 2024-01-02 10:52:26

Z-D-Phe-OH Structure
Z-D-Phe-OH structure
Common Name Z-D-Phe-OH
CAS Number 2448-45-5 Molecular Weight 299.321
Density 1.2±0.1 g/cm3 Boiling Point 511.5±50.0 °C at 760 mmHg
Molecular Formula C17H17NO4 Melting Point 80-82ºC
MSDS Chinese USA Flash Point 263.1±30.1 °C

 Use of Z-D-Phe-OH


((Benzyloxy)carbonyl)-D-phenylalanine is a phenylalanine derivative[1].

 Names

Name (2R)-3-phenyl-2-(phenylmethoxycarbonylamino)propanoic acid
Synonym More Synonyms

 Z-D-Phe-OH Biological Activity

Description ((Benzyloxy)carbonyl)-D-phenylalanine is a phenylalanine 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):1793-823.

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 511.5±50.0 °C at 760 mmHg
Melting Point 80-82ºC
Molecular Formula C17H17NO4
Molecular Weight 299.321
Flash Point 263.1±30.1 °C
Exact Mass 299.115753
PSA 75.63000
LogP 3.58
Vapour Pressure 0.0±1.4 mmHg at 25°C
Index of Refraction 1.591
Storage condition −20°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Safety Phrases 24/25
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%

 Articles8

More Articles
Effects of metalloendoproteinase inhibitors on secretion and intracellular free calcium in bovine adrenal chromaffin cells.

Biochim. Biophys. Acta 889(1) , 1-5, (1986)

The possible role of metalloendoproteinase in stimulus-secretion coupling in adrenal chromaffin cells was examined using the metalloendoproteinase inhibitors 1,10-phenanthroline and carbobenzoxy-Gly-P...

Mechanism of the binding of Z-L-tryptophan and Z-L-phenylalanine to thermolysin and stromelysin-1 in aqueous solutions.

Biochim. Biophys. Acta 1824(2) , 303-10, (2012)

The chemical shift of the carboxylate carbon of Z-tryptophan is increased from 179.85 to 182.82 ppm and 182.87 ppm on binding to thermolysin and stromelysin-1 respectively. The chemical shift of Z-phe...

Modification of a zinc proteinase from Bacillus mesentericus strain 76 by diethylpyrocarbonate.

Int. J. Pept. Protein Res. 37(4) , 325-30, (1991)

Diethylpyrocarbonate (DEPC) inactivated the neutral zinc proteinase from Bacillus mesentericus strain 76/Bacillus subtilis (MCP 76) by ethoxycarbonylation completely. Exposure of the enzyme to DEPC to...

 Synonyms

N-Cbz-D-phenylalanine Z-D-phenylalanine
EINECS 258-154-1
MFCD00063151
L-Phenylalanine, N-[(phenylmethoxy)carbonyl]-
Cbz-D-Phenylalanine
Z-D-phenylalanine
Cbz-protected D-phenylalanine
Phenylalanine, N-[(phenylmethoxy)carbonyl]-
N-CBZ-L-phenylalanine
N-[(Benzyloxy)carbonyl]phenylalanine
(2R)-2-{[(benzyloxy)carbonyl]amino}-3-phenylpropanoic acid
N-Cbz-D-Phenylalanine
Cbz-D-Phe-OH
N-carbobenzyloxy-dl-phenylalanine
N-CARBOBENZYLOXY-D-PHENYLALANINE
Z-D-Phe-OH
(2S)-2-{[(benzyloxy)carbonyl]amino}-3-phenylpropanoic acid
N-Carbobenzoxy-D-phenylalanine
Benzyloxycarbonyl-D-phenylalanine
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