5-Bromopyrimidine-2-carbonitrile

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Reagent Code: #144352
label
Alias 5-Bromopyrimidine-2-nitrile
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CAS Number 38275-57-9

science Other reagents with same CAS 38275-57-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 183.99 g/mol
Formula C₅H₂BrN₃
badge Registry Numbers
MDL Number MFCD02940446
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds for drug discovery. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig to introduce pyrimidine scaffolds into bioactive molecules. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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Test Parameter Specification
Purity 96.5-100
Appearance White to yellow solid
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿174.00
inventory 5g
10-20 days ฿1,030.00
inventory 25g
10-20 days ฿4,420.00
inventory 1g
10-20 days ฿350.00

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5-Bromopyrimidine-2-carbonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds for drug discovery. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig to introduce pyrimidine scaffolds into bioactive molecules. Also utilized in agrochemical research for designing novel pesticides with improved effi

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds for drug discovery. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig to introduce pyrimidine scaffolds into bioactive molecules. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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