3-Bromo-5-nitropicolinonitrile

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Reagent Code: #45295
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CAS Number 573762-54-6

science Other reagents with same CAS 573762-54-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.0030 g/mol
Formula C₆H₂BrN₃O₂
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MDL Number MFCD24847956
inventory_2 Storage & Handling
Storage room temperature

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Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structure is particularly valuable in creating compounds with potential therapeutic applications, such as enzyme inhibitors or receptor modulators. Additionally, it is employed in organic synthesis for constructing complex heterocyclic frameworks, which are essential in drug discovery and material science. The nitro, bromo, and cyano groups on the pyridine ring make it a versatile building block for further functionalization through substitution reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,916.00

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3-Bromo-5-nitropicolinonitrile
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Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structure is particularly valuable in creating compounds with potential therapeutic applications, such as enzyme inhibitors or receptor modulators. Additionally, it is employed in organic synthesis for constructing complex heterocyclic frameworks, which are essential in drug discovery and material science. The nitro, bromo, and cyano groups on the pyri

Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structure is particularly valuable in creating compounds with potential therapeutic applications, such as enzyme inhibitors or receptor modulators. Additionally, it is employed in organic synthesis for constructing complex heterocyclic frameworks, which are essential in drug discovery and material science. The nitro, bromo, and cyano groups on the pyridine ring make it a versatile building block for further functionalization through substitution reactions.

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