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Home  > Chemistry  > Heterocyclic Building Blocks  > Benzimidazoles  > 6-(2-Chloro-5-fluoropyrimidin-4-yl)-4-fluoro-1-isopropyl-2-methyl-1h-benzo[d]imidazole

AA25905

1231930-42-9 | 6-(2-Chloro-5-fluoropyrimidin-4-yl)-4-fluoro-1-isopropyl-2-methyl-1h-benzo[d]imidazole

Packsize Purity Availability Price Discounted Price    Quantity
1g 97% in stock $34.00 $24.00 -   +
5g 97% in stock $43.00 $31.00 -   +
10g 97% in stock $80.00 $56.00 -   +
25g 97% in stock $185.00 $130.00 -   +

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*All prices are in USD.

Description
Catalog Number: AA25905
Chemical Name: 6-(2-Chloro-5-fluoropyrimidin-4-yl)-4-fluoro-1-isopropyl-2-methyl-1h-benzo[d]imidazole
CAS Number: 1231930-42-9
Molecular Formula: C15H13ClF2N4
Molecular Weight: 322.7403
MDL Number: MFCD25977328
SMILES: Clc1ncc(c(n1)c1cc(F)c2c(c1)n(C(C)C)c(n2)C)F

 

Computed Properties
Complexity: 400  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 22  
Hydrogen Bond Acceptor Count: 5  
Rotatable Bond Count: 2  
XLogP3: 3.6  

 

 

Upstream Synthesis Route
  • 6-(2-Chloro-5-fluoropyrimidin-4-yl)-4-fluoro-1-isopropyl-2-methyl-1H-benzimidazole is a versatile compound that finds significant application in chemical synthesis processes. This compound serves as a valuable building block in the creation of novel pharmaceuticals, agrochemicals, and materials. Its unique structural properties make it a crucial component in the development of diverse chemical entities.In chemical synthesis, 6-(2-Chloro-5-fluoropyrimidin-4-yl)-4-fluoro-1-isopropyl-2-methyl-1H-benzimidazole acts as a key intermediate that enables the synthesis of complex molecules with enhanced biological activities. By incorporating this compound into synthetic pathways, chemists can access a wide range of derivatives and analogs that possess tailored properties for specific applications.Furthermore, the strategic placement of functional groups on 6-(2-Chloro-5-fluoropyrimidin-4-yl)-4-fluoro-1-isopropyl-2-methyl-1H-benzimidazole allows for precise manipulation of its reactivity and selectivity during chemical transformations. This control over reactivity makes it an indispensable tool in the hands of synthetic chemists aiming to construct intricate molecular architectures efficiently and with high precision.
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