| Identification | Back Directory | [Name]
3-Bromo-L-tyrosine | [CAS]
38739-13-8 | [Synonyms]
H-Tyr(3-Br)-OH
L-3-Bromotyrosine
3-Bromo-L-tyrosine
L-Tyrosine, 3-bromo-
(S)-2-amino-3-(3-bromo-4-hydroxyphenyl)propanoic acid | [Molecular Formula]
C9H10BrNO3 | [MDL Number]
MFCD09836116 | [MOL File]
38739-13-8.mol | [Molecular Weight]
260.08 |
| Chemical Properties | Back Directory | [Melting point ]
247-248 °C | [Boiling point ]
402.8±45.0 °C(Predicted) | [density ]
1.710±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
Aqueous Acid (Sparingly), DMSO (Heated), Methanol (Heated) | [form ]
Solid | [pka]
2.21±0.20(Predicted) | [color ]
White to Pale Brown |
| Hazard Information | Back Directory | [Uses]
3-Bromo-L-tyrosine is used in the preparation and synthesis of polyclonal antibodies that work against brominated protein related allergic responses and afflictions. Also effective in asthma control a
nd prediction in children. | [Definition]
ChEBI: 3-bromo-L-tyrosine is a bromoamino acid comprising an L-tyrosine core with a bromo- substituent ortho to the hydroxy group on the benzene ring. It is a bromoamino acid, a L-tyrosine derivative, a member of bromobenzenes and a non-proteinogenic L-alpha-amino acid. It is a tautomer of a 3-bromo-L-tyrosine zwitterion. | [Synthesis]
The general procedure for the synthesis of (S)-2-amino-3-(3-bromo-4-hydroxyphenyl)propionic acid from L-tyrosine was as follows: reaction of D- or L-tyrosine (1.0 g) with N-bromosuccinimide (NBS, 1.5 g, 8.3 mmol) in anhydrous THF (15 mL). The reaction mixture was stirred overnight at room temperature. Upon completion of the reaction, the solution was concentrated under reduced pressure and purified by rapid column chromatography on silica gel to afford D- or L-3-bromotyrosine (100 mg). The product was analyzed by electrospray mass spectrometry (positive ion mode) and showed m/z 260/262 (1:1).1H NMR (500 MHz, CD3OD) data were as follows: δH 7.46 (s, H-2); 7.13 (d, J = 8.2 Hz, H-6); 6.91 (d, J = 8.2 Hz, H-5); 3.97 (m, H-8); 3.22 (dd, J = 4.6, 14.6 Hz, H-7a); 3.03 (dd, J = 7.8, 14.6 Hz, H-7b). | [References]
[1] Amino Acids, 2013, vol. 44, # 2, p. 529 - 532
[2] Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie, 1925, vol. 144, p. 250
[3] Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie, 1925, vol. 144, p. 250
[4] Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie, 1925, vol. 144, p. 250
[5] Patent: US2007/259883, 2007, A1. Location in patent: Page/Page column 8 |
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J & K SCIENTIFIC LTD.
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18210857532 18210857532 |
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https://www.jkchemical.com |
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China Langchem Inc.
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0086-21-58956006 |
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www.chemicalbook.com/ShowSupplierProductsList19141/0_EN.htm |
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parabiochem
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025-83453382-8005 |
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www.parabiochem.cn |
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