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AD33345

417721-69-8 | 4-Chloro-3-iodopyridin-2-amine

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $9.00 $6.00 -   +
1g 98% in stock $23.00 $16.00 -   +
5g 98% in stock $70.00 $49.00 -   +
10g 98% in stock $128.00 $89.00 -   +
25g 98% in stock $286.00 $200.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AD33345
Chemical Name: 4-Chloro-3-iodopyridin-2-amine
CAS Number: 417721-69-8
Molecular Formula: C5H4ClIN2
Molecular Weight: 254.45612999999997
MDL Number: MFCD08741521
SMILES: Clc1ccnc(c1I)N

 

Computed Properties
Complexity: 101  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
XLogP3: 1.8  

 

 

Upstream Synthesis Route
  • 2-Pyridinamine, 4-chloro-3-iodo-, is a versatile chemical compound widely utilized in organic synthesis processes. Known for its unique properties, this compound plays a crucial role in the creation of various pharmaceuticals, agrochemicals, and other chemical products. Its reactivity and structural characteristics make it a valuable building block in the synthesis of complex molecules.In chemical synthesis, 2-Pyridinamine, 4-chloro-3-iodo-, serves as a key intermediate for the introduction of functional groups such as chloro and iodo into organic molecules. This compound is particularly useful in the modification of aromatic systems, where the chloro and iodo substituents can greatly influence the overall reactivity and properties of the final product.Additionally, the presence of both chlorine and iodine atoms in the molecule allows for further derivatization through various synthetic reactions, enabling chemists to tailor the structure of the target molecule for specific applications. This compound's versatility and compatibility with a wide range of reagents make it a valuable tool for the construction of diverse chemical structures with precise control over regioselectivity and stereochemistry.
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