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2-Bromo-5-hydroxypyrazine

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Products Intro: Product Name:5-Bromopyrazin-2-ol
CAS:374063-92-0
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Products Intro: Product Name:2-Bromo-5-hydroxypyrazine
CAS:374063-92-0
Purity:97% Package:10G 100G 1KG 25KG
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Products Intro: Product Name:2-Bromo-5-hydroxypyrazine
CAS:374063-92-0

2-Bromo-5-hydroxypyrazine manufacturers

  • 5-Bromopyrazin-2-ol
  • 5-Bromopyrazin-2-ol pictures
  • $2.20 / 100kg
  • 2025-10-13
  • CAS:374063-92-0
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 100kg
2-Bromo-5-hydroxypyrazine Basic information
Uses
Product Name:2-Bromo-5-hydroxypyrazine
Synonyms:5-BROMO-2-PYRAZINOL;5-BROMO-2-HYDROXYPYRAZINE;5-BROMO-2-HYDROXYPYRAZINE,5-BROMO-2-PYRAZINOL;5-bromopyrazin-2-ol;5-bromopyrazin-2-o;2(1H)-Pyrazinone, 5-bromo- 2-Bromo-5-hydroxypyrazine;5-Bromopyrazin-2(1H)-one;2-hydroxy-5-bromopyrazine
CAS:374063-92-0
MF:C4H3BrN2O
MW:174.98
EINECS:
Product Categories:Piperazine series;Building Blocks;Pyrazine;Building Blocks/Intermediates
Mol File:374063-92-0.mol
2-Bromo-5-hydroxypyrazine Structure
2-Bromo-5-hydroxypyrazine Chemical Properties
Melting point 115-119°C
density 2.00±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
pka10.02±0.40(Predicted)
form Crystalline Powder
color White to light brown
InChIInChI=1S/C4H3BrN2O/c5-3-1-7-4(8)2-6-3/h1-2H,(H,7,8)
InChIKeyITTXBHQAWOFJAI-UHFFFAOYSA-N
SMILESC1(=O)NC=C(Br)N=C1
Safety Information
Hazard Codes Xi,Xn
Risk Statements 22-41
Safety Statements 26-39
WGK Germany 1
HS Code 29339900
MSDS Information
2-Bromo-5-hydroxypyrazine Usage And Synthesis
Uses5-bromo-1H-pyrazin-2-one is a useful research chemical.
Synthesis
2-Amino-5-bromopyrazine

59489-71-3

2-Bromo-5-hydroxypyrazine

374063-92-0

General procedure for the synthesis of 2-bromo-5-hydroxypyrazine from 2-amino-5-bromopyrazine: sodium nitrite (1.35 g, 19.53 mmol) was added to concentrated sulfuric acid (9.8 mL) in batches at 0 °C. The mixture was heated to 50 °C until the sodium nitrite was completely dissolved and subsequently cooled to 0 °C. A solution of 5-bromo-pyrazin-2-ylamine (2.57 g, 14.68 mmol) in concentrated sulfuric acid (14.7 mL) was added slowly and dropwise. The ice bath was removed and the mixture was gradually warmed to room temperature and stirred for 15 minutes, followed by heating to 45 °C for 7 minutes. Upon completion of the reaction, it was cooled to room temperature and the reaction mixture was slowly poured into crushed ice water (100 mL). The pH of the aqueous phase was adjusted to 4 with 20% aqueous sodium hydroxide, followed by extraction with ethyl acetate (3 x 100 mL). The organic phases were combined, washed with water (50 mL), dried over anhydrous magnesium sulfate, filtered and concentrated to give 2-bromo-5-hydroxypyrazine (1.88 g, 73% yield) as a yellow solid. The product was characterized by 1H NMR (CDCl3, 300 MHz): δ 8.07 (1H, s), 7.62 (1H, d, J=3.0 Hz).

References[1] Patent: US2005/187266, 2005, A1
[2] Patent: WO2004/92145, 2004, A1. Location in patent: Page 133
[3] Patent: US2010/29650, 2010, A1. Location in patent: Page/Page column 64
[4] Patent: US2005/9838, 2005, A1. Location in patent: Page 150
[5] Journal of Chemical Research, 2005, # 11, p. 747 - 749
2-Bromo-5-hydroxypyrazine Preparation Products And Raw materials
Raw materials2-Amino-5-bromopyrazine-->Sodium hydroxide-->Sulfuric acid-->Sodium nitrite
Preparation Products2-Bromo-5-fluoropyrazine
Tag:2-Bromo-5-hydroxypyrazine(374063-92-0) Related Product Information
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