3-Fluorobenzyl bromide
95%
- Product Code: 117715
Alias:
3-fluorobenzyl bromide; m-fluorobenzyl bromide, α-bromo-3-fluorotoluene
CAS:
456-41-7
Molecular Weight: | 189.02 g./mol | Molecular Formula: | C₇H₆BrF |
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EC Number: | 207-263-2 | MDL Number: | MFCD00000340 |
Melting Point: | Boiling Point: | 88 °C20 mm Hg(lit.) | |
Density: | 1.541 g/mL at 25 °C(lit.) | Storage Condition: | 2~8°C |
Product Description:
Used primarily as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a key building block for introducing the 3-fluorobenzyl group into target molecules, enhancing their biological activity or modifying their properties. In medicinal chemistry, it is employed to develop compounds with potential therapeutic effects, such as enzyme inhibitors or receptor modulators. Additionally, it finds application in the synthesis of specialty chemicals and advanced materials, where its fluorine-substituted aromatic structure contributes to unique chemical behaviors and stability.
Product Specification:
Test | Specification |
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Purity (GC) | 95-100 |
Refractive Index N20/D | 1.545-1.548 |
Specific Gravity (20/20 Degree Celsius) | 1.523-1.545 |
Appearance | Colorless To Yellow Liquid |
Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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5.000 | 10-20 days | ฿330.00 |
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25.000 | 10-20 days | ฿830.00 |
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100.000 | 10-20 days | ฿2,960.00 |
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3-Fluorobenzyl bromide
Used primarily as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a key building block for introducing the 3-fluorobenzyl group into target molecules, enhancing their biological activity or modifying their properties. In medicinal chemistry, it is employed to develop compounds with potential therapeutic effects, such as enzyme inhibitors or receptor modulators. Additionally, it finds application in the synthesis of specialty chemicals and advanced materials, where its fluorine-substituted aromatic structure contributes to unique chemical behaviors and stability.
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