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112883-29-1

112883-29-1 structure
112883-29-1 structure
  • Name: Fmoc-D-Tyr-OH
  • Chemical Name: (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(4-hydroxyphenyl)propanoic acid
  • CAS Number: 112883-29-1
  • Molecular Formula: C24H21NO5
  • Molecular Weight: 403.42700
  • Catalog: Biochemical Amino acids and their derivatives Tyrosine derivatives
  • Create Date: 2018-04-03 08:00:00
  • Modify Date: 2024-01-04 15:58:47
  • (((9H-Fluoren-9-yl)methoxy)carbonyl)-D-tyrosine is a tyrosine derivative[1].

Name (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(4-hydroxyphenyl)propanoic acid
Synonyms D-Tyrosine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
9-fluorenylmethyloxycarbonyl tyrosine
Fmoc-tyrosine
N-Fmoc-D-tyrosine
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-tyrosine
Fmoc-D-tyrosine
Fmoc-L-tyrosine
Fmoc-L-phe(4-OH)-OH
N-Fmoc-L-tyrosine
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-tyrosine
FMOC-D-TYR-OH
Fmoc-L-Tyr-OH
N-Fmoc-L-tyrosine-OH
L-Tyrosine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
Description (((9H-Fluoren-9-yl)methoxy)carbonyl)-D-tyrosine 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.

Density 1.336g/cm3
Boiling Point 672.6ºC at 760 mmHg
Melting Point 175-180℃
Molecular Formula C24H21NO5
Molecular Weight 403.42700
Flash Point 360.6ºC
Exact Mass 403.14200
PSA 95.86000
LogP 4.31750
Appearance Solid | White
Vapour Pressure 5.24E-19mmHg at 25°C
Index of Refraction 1.651
Storage condition Store at RT.
HS Code 29225090

~86%

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112883-29-1

Literature: Djedaini-Pilard, Florence; Azaroual-Bellanger, Nathalie; Gosnat, Muriel; Vernet, Delphine; Perly, Bruno Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1995 , # 4 p. 723 - 730

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Literature: Roviello, Giovanni N.; Musumeci, Domenica; Bucci, Enrico M.; Pedone, Carlo International Journal of Pharmaceutics, 2011 , vol. 415, # 1-2 p. 206 - 210

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Literature: WO2006/37113 A2, ; Page/Page column title page; 5; 13; 14; 24; sheet 5 ;

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112883-29-1

Literature: Ibrahim, Tarek S.; Tala, Srinivasa R.; El-Feky, Said A.; Abdel-Samii, Zakaria K.; Katritzky, Alan R. Synlett, 2011 , # 14 art. no. S03511ST, p. 2013 - 2016

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Literature: US4822890 A1, ;

~78%

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Literature: Di Gioia, Maria Luisa; Leggio, Antonella; Le Pera, Adolfo; Liguori, Angelo; Perri, Francesca; Siciliano, Carlo European Journal of Organic Chemistry, 2004 , # 21 p. 4437 - 4441

~70%

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Literature: Schoen, Istvan; Kisfaludy, Lajos Synthesis, 1986 , # 4 p. 303 - 305

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Literature: Tetrahedron Letters, , vol. 30, # 45 p. 6229 - 6232

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Literature: Synlett, , # 14 art. no. S03511ST, p. 2013 - 2016