2-AMINO-5-BROMO-4-PHENYLPYRIMIDINE

Product Name: 2-AMINO-5-BROMO-4-PHENYLPYRIMIDINE
CAS No.: 85658-55-5
Chemical Name: 2-AMINO-5-BROMO-4-PHENYLPYRIMIDINE
Synonyms: 5-bromo-4-phenylpyrimidin-2-amine;2-AMINO-5-BROMO-4-PHENYLPYRIMIDINE;5-bromo-2-amino-4-phenylpyrimidine;2-Pyrimidinamine, 5-bromo-4-phenyl-
CBNumber: CB82453730
Molecular Formula: C10H8BrN3
Formula Weight: 250.09
MOL File: 85658-55-5.mol

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2-AMINO-5-BROMO-4-PHENYLPYRIMIDINE Property

Boiling point:: 432.9±37.0 °C(Predicted)
Density: 1.566±0.06 g/cm3(Predicted)
storage temp.: Keep in dark place,Inert atmosphere,Room temperature
pka: 1.89±0.10(Predicted)

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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC

Product number: A594885
Product name: 2-Amino-5-bromo-4-phenylpyrimidine
Packaging: 25mg
Price: $45
Updated: 2021/12/16

TRC

Product number: A594885
Product name: 2-Amino-5-bromo-4-phenylpyrimidine
Packaging: 250mg
Price: $170
Updated: 2021/12/16

Biosynth Carbosynth

Product number: FA142051
Product name: 2-Amino-5-bromo-4-phenylpyrimidine
Packaging: 100mg
Price: $70
Updated: 2021/12/16

AK Scientific

Product number: W8815
Product name: 2-Amino-5-bromo-4-phenylpyrimidine
Packaging: 100mg
Price: $132
Updated: 2021/12/16

Biosynth Carbosynth

Product number: FA142051
Product name: 2-Amino-5-bromo-4-phenylpyrimidine
Packaging: 250mg
Price: $140
Updated: 2021/12/16

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2-AMINO-5-BROMO-4-PHENYLPYRIMIDINE Chemical Properties,Usage,Production

Synthesis

2305-87-5

85658-55-5

To a 100 mL round bottom flask was added 4-phenylpyrimidin-2-amine (0.4 g, 0.0023 mol) and a solvent mixture of acetonitrile and chloroform (1:1, 20 mL). Subsequently, N-bromosuccinimide (0.499 g, 0.0028 mol) was added to the same flask. The reaction mixture was stirred at room temperature for 20 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure to give the residue. The residue was extracted by partitioning between ethyl acetate and water. The organic layer was separated, washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give the crude product. The crude product was purified by column chromatography using 60-120 mesh silica gel as stationary phase and 40% hexane solution of ethyl acetate as eluent to give 2-amino-5-bromo-4-phenylpyrimidine [0.3 g, 51% yield]. The product was confirmed by NMR hydrogen spectroscopy (300 MHz, DMSO-d6): δ 8.43 (s, 1H), 7.65-7.61 (m, 2H), 7.49-7.42 (m, 3H), 6.97 (brs, 2H); Liquid Chromatography-Mass Spectrometry (LC-MS) analysis showed that [M+2H]+ m/z 251.9.

References

[1] Chemistry of Heterocyclic Compounds (New York, NY, United States), 1983, p. 91 - 94
[2] Khimiya Geterotsiklicheskikh Soedinenii, 1983, vol. 19, # 1, p. 102 - 106
[3] Patent: WO2014/125426, 2014, A1. Location in patent: Page/Page column 55; 56
[4] Patent: US2005/54590, 2005, A1. Location in patent: Page/Page column 41

2-AMINO-5-BROMO-4-PHENYLPYRIMIDINE Preparation Products And Raw materials

Raw materials

Preparation Products

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2-AMINO-5-BROMO-4-PHENYLPYRIMIDINE Suppliers

China 31 Germany 1 India 1 United Kingdom 1 United States 5 Global 39

Pure Chemistry Scientific Inc.

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85658-55-5, 2-AMINO-5-BROMO-4-PHENYLPYRIMIDINERelated Search:

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2-AMINO-5-BROMO-4-PHENYLPYRIMIDINE

5-bromo-4-phenylpyrimidin-2-amine

5-bromo-2-amino-4-phenylpyrimidine

2-Pyrimidinamine, 5-bromo-4-phenyl-

85658-55-5

Heterocycle-Pyrimidine series