4-Chloro-3-fluorobenzyl bromide
98%
- Product Code: 119127
Alias:
4-Chloro-3-fluorobenzyl bromide
CAS:
206362-80-3
| Molecular Weight: | 223.47 g./mol | Molecular Formula: | C₇H₅BrClF |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04115859 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
Used primarily as an intermediate in organic synthesis, this compound is valuable in the production of pharmaceuticals and agrochemicals. It serves as a key building block for the development of active ingredients in drugs, particularly those targeting specific biological pathways. Additionally, it is employed in the creation of complex molecules for crop protection agents, helping to enhance the efficacy and specificity of these products. Its reactive benzyl bromide group makes it useful in coupling reactions, enabling the formation of carbon-carbon or carbon-heteroatom bonds in various synthetic processes.
Product Specification:
| Test | Specification |
|---|---|
| Melting Point | 30-33 |
| Purity (Argentmetric Titration) | 97.5-102.5 |
| Purity (GC) | 98 |
| Appearance | White To Cream Powder Or Crystals |
| Infrared Spectrum | Conforms To Structure |
| Note | This Product Is Low Melting Point Solid, May Change State In Different Environments (Solid, Liquid Or Semi-Solid) |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿390.00 |
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| 5.000 | 10-20 days | ฿1,460.00 |
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| 25.000 | 10-20 days | ฿6,500.00 |
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4-Chloro-3-fluorobenzyl bromide
Used primarily as an intermediate in organic synthesis, this compound is valuable in the production of pharmaceuticals and agrochemicals. It serves as a key building block for the development of active ingredients in drugs, particularly those targeting specific biological pathways. Additionally, it is employed in the creation of complex molecules for crop protection agents, helping to enhance the efficacy and specificity of these products. Its reactive benzyl bromide group makes it useful in coupling reactions, enabling the formation of carbon-carbon or carbon-heteroatom bonds in various synthetic processes.
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