logo
Home  > Chemistry  > Heterocyclic Building Blocks  > Pyridines  > 2-Aminomethyl-3-fluoropyridine dihydrochloride

AB51598

312904-49-7 | 2-Aminomethyl-3-fluoropyridine dihydrochloride

Packsize Purity Availability Price Discounted Price    Quantity
1g 95% in stock $16.00 $12.00 -   +
5g 95% in stock $65.00 $45.00 -   +
10g 95% in stock $125.00 $88.00 -   +
25g 95% in stock $183.00 $129.00 -   +
50g 95% in stock $294.00 $206.00 -   +
100g 95% in stock $471.00 $330.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB51598
Chemical Name: 2-Aminomethyl-3-fluoropyridine dihydrochloride
CAS Number: 312904-49-7
Molecular Formula: C6H9Cl2FN2
Molecular Weight: 199.0535
MDL Number: MFCD09954760
SMILES: NCc1ncccc1F.Cl.Cl

 

Computed Properties
Complexity: 87.1  
Covalently-Bonded Unit Count: 3  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 3  
Rotatable Bond Count: 1  

 

 

Upstream Synthesis Route
  • The (3-fluoropyridin-2-yl)methanamine dihydrochloride is a versatile compound widely used in chemical synthesis processes. Its unique structure and properties make it valuable for various applications, particularly in the field of organic chemistry.This compound serves as an important building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its presence as a functional group allows for selective reactions and modifications, enabling the formation of complex molecular structures with high efficiency and precision.In organic synthesis, (3-fluoropyridin-2-yl)methanamine dihydrochloride can be utilized as a key intermediate in the production of diverse compounds, including heterocyclic derivatives and biologically active molecules. Its incorporation into synthetic pathways often leads to improved yields, selectivity, and overall synthetic efficiency.Furthermore, this compound's ability to participate in a range of transformations, such as substitution, addition, and condensation reactions, makes it a valuable tool for synthetic chemists looking to streamline their processes and access novel chemical entities.
FEATURED PRODUCTS