Basic information Safety Supplier Related

3-Bromo-L-tyrosine

Basic information Safety Supplier Related

3-Bromo-L-tyrosine Basic information

Product Name:
3-Bromo-L-tyrosine
Synonyms:
  • 3-Bromo-L-tyrosine
  • H-Tyr(3-Br)-OH
  • L-3-Bromotyrosine
  • (S)-2-amino-3-(3-bromo-4-hydroxyphenyl)propanoic acid
  • L-Tyrosine, 3-bromo-
  • (2S)-2-amino-3-(3-bromo-4-hydroxyphenyl)propanoic acid
  • 3-bromo-L-tyrosine (L-type)
CAS:
38739-13-8
MF:
C9H10BrNO3
MW:
260.08
Mol File:
38739-13-8.mol
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3-Bromo-L-tyrosine Chemical Properties

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
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3-Bromo-L-tyrosine Usage And Synthesis

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

60-18-4

38739-13-8

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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