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Home  > 2-Amino-3-bromo-4-picoline

AB60982

40073-38-9 | 2-Amino-3-bromo-4-picoline

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $17.00 $12.00 -   +
1g 95% in stock $26.00 $18.00 -   +
5g 95% in stock $85.00 $60.00 -   +
10g 95% in stock $146.00 $103.00 -   +
100g 95% in stock $1,395.00 $977.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB60982
Chemical Name: 2-Amino-3-bromo-4-picoline
CAS Number: 40073-38-9
Molecular Formula: C6H7BrN2
Molecular Weight: 187.0372
MDL Number: MFCD08061297
SMILES: Cc1ccnc(c1Br)N

 

Computed Properties
Complexity: 97.1  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
XLogP3: 1.6  

 

 

Upstream Synthesis Route
  • 3-Bromo-4-methyl-2-pyridinamine, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role as a key building block in organic chemistry reactions. Its unique structure and reactivity make it an essential intermediate in the production of various pharmaceuticals, agrochemicals, and materials.One of the primary applications of 3-Bromo-4-methyl-2-pyridinamine is in the synthesis of heterocyclic compounds. This compound serves as a valuable starting material for the preparation of complex molecules with heterocyclic moieties, which are commonly found in bioactive compounds and natural products. By undergoing various transformations and functionalizations, 3-Bromo-4-methyl-2-pyridinamine can be used to introduce different substituents and functional groups onto the pyridine ring, enabling the synthesis of diverse chemical structures.Furthermore, 3-Bromo-4-methyl-2-pyridinamine is often employed in transition metal-catalyzed coupling reactions. It can participate in palladium-catalyzed cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, to facilitate the formation of carbon-carbon bonds. These transformations are valuable tools in modern organic synthesis for creating complex molecules efficiently and selectively.Overall, the versatility and reactivity of 3-Bromo-4-methyl-2-pyridinamine make it a valuable tool in chemical synthesis, enabling the construction of intricate molecular structures with diverse functionalities.
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