alpha-Methyl-5-methoxy-2-nitro-4-(2-propyn-1-yloxy)benzyl Alcohol
95%
- Product Code: 85606
CAS:
1255792-05-2
| Molecular Weight: | 251.24 g./mol | Molecular Formula: | C₁₂H₁₃NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31619535 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the synthesis of advanced organic materials and specialized chemical intermediates. Its unique structure, featuring a nitro group and a propynyloxy moiety, makes it valuable in the development of photoactive compounds and light-sensitive polymers. It is often employed in research focused on creating novel dyes, pigments, and coatings with enhanced optical properties. Additionally, it serves as a key building block in the preparation of pharmaceutical intermediates, particularly in the design of molecules with potential biological activity. Its reactivity and functional groups also make it suitable for use in organic synthesis and catalysis studies.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | white to yellow solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿6,840.00 |
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| 1.000 | 10-20 days | ฿16,200.00 |
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alpha-Methyl-5-methoxy-2-nitro-4-(2-propyn-1-yloxy)benzyl Alcohol
This compound is primarily utilized in the synthesis of advanced organic materials and specialized chemical intermediates. Its unique structure, featuring a nitro group and a propynyloxy moiety, makes it valuable in the development of photoactive compounds and light-sensitive polymers. It is often employed in research focused on creating novel dyes, pigments, and coatings with enhanced optical properties. Additionally, it serves as a key building block in the preparation of pharmaceutical intermediates, particularly in the design of molecules with potential biological activity. Its reactivity and functional groups also make it suitable for use in organic synthesis and catalysis studies.
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