1,4-Dibromonaphthalene
98%
- Product Code: 114179
Alias:
1,4-Dibromonaphthalene
CAS:
83-53-4
Molecular Weight: | 285.96 g./mol | Molecular Formula: | C₁₀H₆Br₂ |
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EC Number: | MDL Number: | MFCD00041823 | |
Melting Point: | 80-82 °C | Boiling Point: | |
Density: | Storage Condition: | room temperature |
Product Description:
1,4-Dibromonaphthalene is primarily used in organic synthesis as a building block for more complex chemical compounds. It serves as a key intermediate in the production of naphthalene derivatives, which are important in the development of dyes, pigments, and fluorescent materials. Additionally, it is utilized in the synthesis of organic semiconductors and liquid crystals, which are essential components in electronic displays and photovoltaic devices. The compound also finds application in research laboratories for studying reaction mechanisms and developing new chemical processes. Its bromine atoms make it a versatile reagent for various cross-coupling reactions, enabling the creation of diverse organic molecules.
Product Specification:
Test | Specification |
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Melting Point | 80-84 |
Purity (GC) | 98-100 |
Appearance | Light Orange-Brown Crystalline Powder |
Infrared Spectrum | Conforms To Structure |
Solubility In Hot Methanol | Almost Transparency |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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5.000 | 10-20 days | $11.80 |
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25.000 | 10-20 days | $46.01 |
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100.000 | 10-20 days | $180.90 |
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500.000 | 10-20 days | $768.43 |
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1,4-Dibromonaphthalene
1,4-Dibromonaphthalene is primarily used in organic synthesis as a building block for more complex chemical compounds. It serves as a key intermediate in the production of naphthalene derivatives, which are important in the development of dyes, pigments, and fluorescent materials. Additionally, it is utilized in the synthesis of organic semiconductors and liquid crystals, which are essential components in electronic displays and photovoltaic devices. The compound also finds application in research laboratories for studying reaction mechanisms and developing new chemical processes. Its bromine atoms make it a versatile reagent for various cross-coupling reactions, enabling the creation of diverse organic molecules.
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