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6636-78-8

2-Chloro-3-hydroxypyridine

Catalog#: AR0033WH  |   CAS#: 6636-78-8  |   MDL#: MFCD00006235  |   MF: C5H4ClNO  |   MW: 129.5444

Packsize Purity Price Availability Quantity
1g 98% $3.00 Global Stock Buy Now Add To Cart
5g 98% $3.00 Global Stock Buy Now Add To Cart
10g 98% $4.00 Global Stock Buy Now Add To Cart
25g 98% $5.00 Global Stock Buy Now Add To Cart
100g 98% $9.00 Global Stock Buy Now Add To Cart
500g 98% $43.00 Global Stock Buy Now Add To Cart
1kg 98% $85.00 Global Stock Buy Now Add To Cart
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Catalog Number AR0033WH
Chemical Name 2-Chloro-3-hydroxypyridine
CAS Number 6636-78-8
Molecular Formula C5H4ClNO
Molecular Weight 129.5444
MDL Number MFCD00006235
SMILES Oc1cccnc1Cl
NSC Number 18469

2-Chloro-3-hydroxypyridine is a versatile compound commonly utilized in chemical synthesis, particularly in the pharmaceutical industry. This compound serves as a valuable building block in the creation of various pharmaceutical agents and intermediates due to its unique structure and reactivity. In organic synthesis, 2-Chloro-3-hydroxypyridine can participate in a range of key reactions, such as nucleophilic substitution, oxidation, and condensation, enabling the formation of complex molecules with specific biological activities.One prominent application of 2-Chloro-3-hydroxypyridine is its use as a precursor in the synthesis of pyridine-based pharmaceuticals. By functionalizing the hydroxyl and chlorine groups present in the molecule, chemists can introduce diverse functional groups or modify the pyridine ring to tailor the properties of the final pharmaceutical product. Additionally, the chloro and hydroxyl groups can serve as handles for further derivatization, allowing for the incorporation of specific functionalities required for biological activity or improved pharmacokinetic properties.Moreover, 2-Chloro-3-hydroxypyridine can also act as a coupling partner in cross-coupling reactions, such as Suzuki-Miyaura or Heck coupling, facilitating the construction of complex structures. Its ability to engage in multiple types of chemical transformations makes it a valuable tool for the preparation of drug candidates and bioactive compounds in medicinal chemistry research and drug discovery efforts.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class N/A
Packing Group N/A

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