(2-Fluorobenzyl)hydrazine Hydrochloride
95%
- Product Code: 80163
CAS:
1216246-45-5
Molecular Weight: | 176.62 g./mol | Molecular Formula: | C₇H₁₀ClFN₂ |
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EC Number: | MDL Number: | MFCD12403346 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, dry |
Product Description:
(2-Fluorobenzyl)hydrazine Hydrochloride is primarily used in organic synthesis as a versatile building block for the preparation of various heterocyclic compounds. It serves as a key intermediate in the development of pharmaceuticals, particularly in the synthesis of molecules with potential biological activity. The compound is often employed in the creation of hydrazone derivatives, which are valuable in medicinal chemistry for designing inhibitors or modulators of specific enzymes or receptors. Additionally, it is utilized in the preparation of fluorinated analogs of bioactive molecules, enhancing their pharmacokinetic properties. Its application extends to research settings where it aids in the study of structure-activity relationships in drug discovery.
Product Specification:
Test | Specification |
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PURITY | 94.5-100 |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿1,030.00 |
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5.000 | 10-20 days | ฿4,140.00 |
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(2-Fluorobenzyl)hydrazine Hydrochloride
(2-Fluorobenzyl)hydrazine Hydrochloride is primarily used in organic synthesis as a versatile building block for the preparation of various heterocyclic compounds. It serves as a key intermediate in the development of pharmaceuticals, particularly in the synthesis of molecules with potential biological activity. The compound is often employed in the creation of hydrazone derivatives, which are valuable in medicinal chemistry for designing inhibitors or modulators of specific enzymes or receptors. Additionally, it is utilized in the preparation of fluorinated analogs of bioactive molecules, enhancing their pharmacokinetic properties. Its application extends to research settings where it aids in the study of structure-activity relationships in drug discovery.
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