2-Chloro-5-(3-methoxyphenyl)pyrazine

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Reagent Code: #166367
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CAS Number 88066-86-8

science Other reagents with same CAS 88066-86-8

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Weight 220.65496 g/mol
Formula C₁₁H₉ClN₂O
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MDL Number MFCD09881459
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Storage Room temperature

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Used in pharmaceutical synthesis as an intermediate for developing bioactive compounds, particularly in the production of kinase inhibitors and antitumor agents. It serves as a building block in the construction of complex heterocyclic systems due to its reactive chloro and aryl substituents. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity. Its methoxyphenyl moiety enhances electron-donating properties, beneficial in tuning the electronic characteristics of final active molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,400.00
inventory 250mg
10-20 days ฿21,500.00
inventory 1g
10-20 days ฿51,550.00

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2-Chloro-5-(3-methoxyphenyl)pyrazine
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Used in pharmaceutical synthesis as an intermediate for developing bioactive compounds, particularly in the production of kinase inhibitors and antitumor agents. It serves as a building block in the construction of complex heterocyclic systems due to its reactive chloro and aryl substituents. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in agrochemical research for designing novel pesticides with improved effi

Used in pharmaceutical synthesis as an intermediate for developing bioactive compounds, particularly in the production of kinase inhibitors and antitumor agents. It serves as a building block in the construction of complex heterocyclic systems due to its reactive chloro and aryl substituents. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity. Its methoxyphenyl moiety enhances electron-donating properties, beneficial in tuning the electronic characteristics of final active molecules.

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