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Home  > Chemistry  > Heterocyclic Building Blocks  > Pyridines  > 2,6-Dichloropyridine-4-methanol

AA07811

101990-69-6 | 2,6-Dichloropyridine-4-methanol

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $8.00 $6.00 -   +
1g 97% in stock $18.00 $13.00 -   +
5g 97% in stock $47.00 $33.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA07811
Chemical Name: 2,6-Dichloropyridine-4-methanol
CAS Number: 101990-69-6
Molecular Formula: C6H5Cl2NO
Molecular Weight: 178.016
MDL Number: MFCD00052638
SMILES: OCc1cc(Cl)nc(c1)Cl

 

Computed Properties
Complexity: 102  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 1  
XLogP3: 1.9  

 

 

Upstream Synthesis Route
  • 2,6-Dichloro-4-Pyridinyl Methanol, also known as $name$, serves a crucial role in chemical synthesis as a versatile building block in the production of various pharmaceuticals, pesticides, and agrochemicals. Its unique molecular structure allows for precise manipulation and functionalization, making it a valuable tool in the development of novel compounds with diverse applications.Due to its reactive nature, 2,6-Dichloro-4-Pyridinyl Methanol is commonly employed as a key intermediate in the synthesis of complex molecules. Its chlorinated pyridine ring provides opportunities for selective chemical modifications, facilitating the creation of tailored compounds with specific properties and functions. By incorporating this compound into synthetic pathways, chemists can access a wide range of potential products with enhanced biological or pesticidal activities.In pharmaceutical synthesis, 2,6-Dichloro-4-Pyridinyl Methanol can be utilized to introduce functional groups or structural motifs that are essential for the activity and pharmacokinetics of a drug candidate. Its presence in the molecular scaffold can influence the compound's solubility, stability, and affinity for biological targets, thereby influencing its therapeutic potential. Furthermore, the versatility of this building block allows for the construction of diverse chemical libraries for screening purposes, enabling the discovery of new drug candidates with improved properties.In the field of agrochemicals, 2,6-Dichloro-4-Pyridinyl Methanol plays a crucial role in the development of novel pesticides and herbicides. By incorporating this compound into the design of crop protection products, chemists can enhance their efficacy, selectivity, and environmental safety. The strategic placement of the chlorinated pyridine moiety in the chemical structure can confer specific modes of action against target pests or weeds, leading to superior performance in agricultural applications.Overall, the application of 2,6-Dichloro-4-Pyridinyl Methanol in chemical synthesis enables the creation of diverse compounds with valuable properties for pharmaceutical, agricultural, and industrial purposes. Its versatility and reactivity make it a valuable building block for the design and optimization of novel molecules with tailored functions and applications.
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