2-(Boc-amino)-5-bromoisonicotinaldehyde

≥95%

Reagent Code: #69840
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CAS Number 1260667-46-6

science Other reagents with same CAS 1260667-46-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 301.14 g/mol
Formula C₁₁H₁₃BrN₂O₃
badge Registry Numbers
MDL Number MFCD18249889
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. It features an aldehyde group at the 4-position of the pyridine ring, which is highly reactive for nucleophilic additions and other transformations. It is particularly valuable in pharmaceutical research, where it serves as a building block for the development of active pharmaceutical ingredients (APIs). The Boc (tert-butoxycarbonyl) protecting group allows for selective reactions at other functional sites, making it useful in peptide synthesis and the creation of heterocyclic compounds. Additionally, the bromo substituent enables further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in drug discovery and material science. Its application extends to the synthesis of ligands for catalysis and the development of novel bioactive compounds.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿17,955.00
inventory 250mg
10-20 days ฿7,299.00

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2-(Boc-amino)-5-bromoisonicotinaldehyde
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This compound is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. It features an aldehyde group at the 4-position of the pyridine ring, which is highly reactive for nucleophilic additions and other transformations. It is particularly valuable in pharmaceutical research, where it serves as a building block for the development of active pharmaceutical ingredients (APIs). The Boc (tert-butoxycarbonyl) protecting group allows for selective reactions at oth

This compound is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. It features an aldehyde group at the 4-position of the pyridine ring, which is highly reactive for nucleophilic additions and other transformations. It is particularly valuable in pharmaceutical research, where it serves as a building block for the development of active pharmaceutical ingredients (APIs). The Boc (tert-butoxycarbonyl) protecting group allows for selective reactions at other functional sites, making it useful in peptide synthesis and the creation of heterocyclic compounds. Additionally, the bromo substituent enables further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in drug discovery and material science. Its application extends to the synthesis of ligands for catalysis and the development of novel bioactive compounds.

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