3-Fluorobenzimidamide hydrochloride
98%
- Product Code: 79426
CAS:
75207-72-6
| Molecular Weight: | 174.6 g./mol | Molecular Formula: | C₇H₈ClFN₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 253°C | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive molecules, particularly in the synthesis of compounds with potential therapeutic applications. Its structure, featuring a fluorinated benzimidamide group, makes it valuable for constructing more complex chemical entities, especially in drug discovery programs targeting enzymes or receptors. Additionally, it can be employed in the preparation of fluorinated heterocycles, which are often explored for their unique biological activities and pharmacokinetic properties. Its use in medicinal chemistry is driven by the ability to introduce fluorine atoms into drug candidates, enhancing their stability, bioavailability, and binding affinity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 10.000 | 10-20 days | ฿7,875.00 |
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3-Fluorobenzimidamide hydrochloride
This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive molecules, particularly in the synthesis of compounds with potential therapeutic applications. Its structure, featuring a fluorinated benzimidamide group, makes it valuable for constructing more complex chemical entities, especially in drug discovery programs targeting enzymes or receptors. Additionally, it can be employed in the preparation of fluorinated heterocycles, which are often explored for their unique biological activities and pharmacokinetic properties. Its use in medicinal chemistry is driven by the ability to introduce fluorine atoms into drug candidates, enhancing their stability, bioavailability, and binding affinity.
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