4-(Chloromethyl)-3-methylpyridine hydrochloride
97%
- Product Code: 46547
CAS:
117934-36-8
Molecular Weight: | 178.06 g./mol | Molecular Formula: | C₇H₉Cl₂N |
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EC Number: | MDL Number: | MFCD20527162 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of various drugs, including antihistamines and anti-inflammatory agents. Its chloromethyl group allows for further functionalization, making it valuable in organic synthesis for creating complex molecules. Additionally, it is employed in research settings for the preparation of pyridine derivatives, which are important in medicinal chemistry for their diverse biological activities. Its role in facilitating the construction of heterocyclic compounds underscores its significance in drug discovery and development processes.
Product Specification:
Test | Specification |
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APPEARANCE | solid |
PURITY | 96.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | $122.70 |
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0.250 | 10-20 days | $214.72 |
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1.000 | 10-20 days | $731.46 |
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5.000 | 10-20 days | $2,666.70 |
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4-(Chloromethyl)-3-methylpyridine hydrochloride
This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of various drugs, including antihistamines and anti-inflammatory agents. Its chloromethyl group allows for further functionalization, making it valuable in organic synthesis for creating complex molecules. Additionally, it is employed in research settings for the preparation of pyridine derivatives, which are important in medicinal chemistry for their diverse biological activities. Its role in facilitating the construction of heterocyclic compounds underscores its significance in drug discovery and development processes.
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