Pyridine-2-carboxylic Acid Hydrochloride
>98.0%(HPLC)
- Product Code: 77986
CAS:
636-80-6
| Molecular Weight: | 159.57 g./mol | Molecular Formula: | C₆H₅NO₂HCl |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00050666 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various drugs, particularly those targeting neurological and cardiovascular conditions. Its role in the production of active pharmaceutical ingredients (APIs) is significant, often contributing to the structural framework of complex molecules. Additionally, it finds application in organic synthesis, aiding in the creation of heterocyclic compounds that are essential in medicinal chemistry. The compound is also utilized in laboratory settings for studying reaction mechanisms and developing new synthetic pathways. Its stability and reactivity make it a valuable reagent in chemical transformations, particularly in the formation of esters and amides.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Almost white powder to crystal |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿880.00 |
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Pyridine-2-carboxylic Acid Hydrochloride
Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various drugs, particularly those targeting neurological and cardiovascular conditions. Its role in the production of active pharmaceutical ingredients (APIs) is significant, often contributing to the structural framework of complex molecules. Additionally, it finds application in organic synthesis, aiding in the creation of heterocyclic compounds that are essential in medicinal chemistry. The compound is also utilized in laboratory settings for studying reaction mechanisms and developing new synthetic pathways. Its stability and reactivity make it a valuable reagent in chemical transformations, particularly in the formation of esters and amides.
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