(5-bromopyridin-3-yl)methanamine

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Reagent Code: #143870
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CAS Number 135124-70-8

science Other reagents with same CAS 135124-70-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.04 g/mol
Formula C₆H₇BrN₂
badge Registry Numbers
MDL Number MFCD06212876
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization in drug molecules, enhancing binding affinity and target specificity. Commonly employed in medicinal chemistry for constructing nitrogen-containing heterocyclic systems. Also utilized in agrochemical research for designing novel active ingredients. The amine group facilitates coupling reactions, making it valuable in combinatorial chemistry and library synthesis for high-throughput screening.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,580.00
inventory 5g
10-20 days ฿11,800.00
inventory 25g
10-20 days ฿46,880.00

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(5-bromopyridin-3-yl)methanamine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization in drug molecules, enhancing binding affinity and target specificity. Commonly employed in medicinal chemistry for constructing nitrogen-containing heterocyclic systems. Also utilized in agrochemical research for designing novel active ingredients. The amine group facilitates coupling reactions, m

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization in drug molecules, enhancing binding affinity and target specificity. Commonly employed in medicinal chemistry for constructing nitrogen-containing heterocyclic systems. Also utilized in agrochemical research for designing novel active ingredients. The amine group facilitates coupling reactions, making it valuable in combinatorial chemistry and library synthesis for high-throughput screening.

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