6-Methoxy-1-tetralone
99%
- Product Code: 50073
Alias:
6-methoxy-1-tetralone 6-methoxy-1,2,3,4-tetralone-1-one 6-methoxy-α-tetralone
CAS:
1078-19-9
Molecular Weight: | 176.21 g./mol | Molecular Formula: | C₁₁H₁₂O₂ |
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EC Number: | 214-078-0 | MDL Number: | MFCD00001695 |
Melting Point: | 77-79 °C(lit.) | Boiling Point: | 171 °C11 mm Hg(lit.) |
Density: | Storage Condition: | 2~8°C |
Product Description:
This compound is primarily used in organic synthesis as a key intermediate in the production of various pharmaceuticals and bioactive molecules. It serves as a building block for the synthesis of tetralin-based compounds, which are often explored for their potential therapeutic properties. Specifically, it is utilized in the development of compounds with anti-inflammatory, anticancer, and central nervous system (CNS) activity. Its methoxy group and tetralone structure make it versatile for modifications, enabling the creation of diverse chemical libraries for drug discovery and development. Additionally, it is employed in research settings to study reaction mechanisms and develop novel synthetic pathways.
Product Specification:
Test | Specification |
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CARBON | 73.8 76.1% |
Melting point | 77 81? |
Purity | 98.5 100% |
APPEARANCE | OFF-WHITE TO YELLOW POWDER |
INFRARED SPECTRUM | Conforms to Structure |
SOLUBILITY IN CHCL3 | CLEARLIGHT TO DARK YELLOW SOLUTION,50MG/ML |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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5.000 | 10-20 days | €8.97 |
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25.000 | 10-20 days | €26.91 |
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100.000 | 10-20 days | €103.42 |
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6-Methoxy-1-tetralone
This compound is primarily used in organic synthesis as a key intermediate in the production of various pharmaceuticals and bioactive molecules. It serves as a building block for the synthesis of tetralin-based compounds, which are often explored for their potential therapeutic properties. Specifically, it is utilized in the development of compounds with anti-inflammatory, anticancer, and central nervous system (CNS) activity. Its methoxy group and tetralone structure make it versatile for modifications, enabling the creation of diverse chemical libraries for drug discovery and development. Additionally, it is employed in research settings to study reaction mechanisms and develop novel synthetic pathways.
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