8-Nitro-3,4-dihydro-2H-1,5-benzodioxepin-7-amine
95%
- Product Code: 56789
CAS:
81864-62-2
| Molecular Weight: | 210.19 g./mol | Molecular Formula: | C₉H₁₀N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02103699 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules. Its structure, featuring a nitro group and an amine group, makes it a versatile building block for constructing complex chemical entities. Researchers often employ it in the synthesis of potential drug candidates, particularly those targeting neurological disorders or infections, due to its unique benzodioxepin core. Additionally, it may be explored for its potential in creating novel materials or dyes, leveraging its aromatic and reactive functional groups. Its applications are largely confined to laboratory settings, where it is used to study chemical reactions and develop new therapeutic agents.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Yellow to orange powder |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿675.00 |
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| 0.100 | 10-20 days | ฿1,881.00 |
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| 0.500 | 10-20 days | ฿6,390.00 |
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| 2.500 | 10-20 days | ฿30,996.00 |
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8-Nitro-3,4-dihydro-2H-1,5-benzodioxepin-7-amine
This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules. Its structure, featuring a nitro group and an amine group, makes it a versatile building block for constructing complex chemical entities. Researchers often employ it in the synthesis of potential drug candidates, particularly those targeting neurological disorders or infections, due to its unique benzodioxepin core. Additionally, it may be explored for its potential in creating novel materials or dyes, leveraging its aromatic and reactive functional groups. Its applications are largely confined to laboratory settings, where it is used to study chemical reactions and develop new therapeutic agents.
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