2-Bromo-3-Nitro-4-Picoline

≥95%

Reagent Code: #146819
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CAS Number 23056-45-3

science Other reagents with same CAS 23056-45-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.02 g/mol
Formula C₆H₅BrN₂O₂
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization, making it valuable in building complex organic molecules. Commonly employed in the development of active ingredients in crop protection products due to the presence of nitro and bromo groups that can undergo further transformation. Also utilized in research laboratories for the preparation of heterocyclic compounds and nitrogen-containing derivatives. The compound’s reactivity supports cross-coupling reactions, enabling the formation of carbon-carbon bonds in fine chemical synthesis.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,410.00
inventory 25g
10-20 days ฿5,250.00
inventory 100g
10-20 days ฿17,840.00
inventory 10g
10-20 days ฿2,560.00

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2-Bromo-3-Nitro-4-Picoline
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization, making it valuable in building complex organic molecules. Commonly employed in the development of active ingredients in crop protection products due to the presence of nitro and bromo groups that can undergo further transformation. Also utilized in research laboratories for the preparation of heterocyclic compounds and nitrogen-containing derivatives. The compound’s reactiv

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization, making it valuable in building complex organic molecules. Commonly employed in the development of active ingredients in crop protection products due to the presence of nitro and bromo groups that can undergo further transformation. Also utilized in research laboratories for the preparation of heterocyclic compounds and nitrogen-containing derivatives. The compound’s reactivity supports cross-coupling reactions, enabling the formation of carbon-carbon bonds in fine chemical synthesis.

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