7-Methoxy-2,3-dihydro-1H-inden-1-amine
≥95%
- Product Code: 62889
CAS:
1032279-33-6
| Molecular Weight: | 163.22 g./mol | Molecular Formula: | C₁₀H₁₃NO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD15527075 | |
| Melting Point: | Boiling Point: | 264.3±40.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure, featuring a methoxy group and an amine functionality, makes it a versatile building block for developing compounds with potential therapeutic applications. It is often employed in the creation of ligands that target specific receptors in the central nervous system, contributing to the development of drugs for neurological disorders. Additionally, its unique scaffold is explored in the design of inhibitors for enzymes involved in disease pathways, particularly in the context of inflammation and cancer. Researchers also leverage its chemical properties to optimize drug candidates for improved bioavailability and efficacy.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €410.53 |
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| 0.250 | 10-20 days | €821.06 |
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7-Methoxy-2,3-dihydro-1H-inden-1-amine
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure, featuring a methoxy group and an amine functionality, makes it a versatile building block for developing compounds with potential therapeutic applications. It is often employed in the creation of ligands that target specific receptors in the central nervous system, contributing to the development of drugs for neurological disorders. Additionally, its unique scaffold is explored in the design of inhibitors for enzymes involved in disease pathways, particularly in the context of inflammation and cancer. Researchers also leverage its chemical properties to optimize drug candidates for improved bioavailability and efficacy.
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