(4-(Aminomethyl)phenyl)(phenyl)methanone hydrochloride
95%
- Product Code: 87539
CAS:
24095-40-7
| Molecular Weight: | 247.72 g./mol | Molecular Formula: | C₁₄H₁₄ClNO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06245504 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8 ℃, inert gas storage |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring both an aminomethyl group and a benzophenone moiety, makes it a valuable building block for creating complex molecules. It is often employed in the preparation of compounds with potential therapeutic applications, such as central nervous system (CNS) agents or anti-inflammatory drugs. Additionally, its reactive sites allow for further functionalization, enabling the creation of diverse chemical libraries for drug discovery and optimization. Its use is typically confined to laboratory settings, where it contributes to the development of novel medications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,300.00 |
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| 0.250 | 10-20 days | ฿9,432.00 |
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| 1.000 | 10-20 days | ฿23,571.00 |
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(4-(Aminomethyl)phenyl)(phenyl)methanone hydrochloride
This compound is primarily utilized in pharmaceutical research and development, particularly as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring both an aminomethyl group and a benzophenone moiety, makes it a valuable building block for creating complex molecules. It is often employed in the preparation of compounds with potential therapeutic applications, such as central nervous system (CNS) agents or anti-inflammatory drugs. Additionally, its reactive sites allow for further functionalization, enabling the creation of diverse chemical libraries for drug discovery and optimization. Its use is typically confined to laboratory settings, where it contributes to the development of novel medications.
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