
Estratetraenol
June 8, 2023
2-(Bromomethyl)thiazole
June 15, 2023Product | Methyl 5-(bromomethyl)-2-fluorobenzoate | ||
CAS No. | 709-45-5 | ||
Synonyms | AB315375;
Methyl 3-(bromomethyl)-2-benzofurancarboxylate; 3-(Bromomethyl)benzofuran-2-carboxylic acid. |
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InChI | 1S/C9H8BrFO2/c1-13-9(12)7-4-6(5-10)2-3-8(7)11/h2-4H,5H2,1H3 | ||
InChI key | GHEFZYZTGHKBBI-UHFFFAOYSA-N | ||
Availability | In Stock | ||
MF. | C9H8BRFO2 | MW. | 247.06 |
Appearance | Liquid | Purity | ≥95% |
Application | For research use only | Storage | 2-8°C |
COA & NMR | Download | MSDS | Download |
Methyl 5-(bromomethyl)-2-fluorobenzoate has a variety of scientific research applications. It has been used as a catalyst in the synthesis of organic compounds, such as α-hydroxy ketones, β-amino alcohols, and β-amino acids. It has also been used as a reagent in the synthesis of heterocyclic compounds, such as pyridines, quinolines, and pyrimidines.
Methyl 5-(bromomethyl)-2-fluorobenzoate is an organobromine compound, and as such, it has been shown to have some biochemical and physiological effects. It has been found to have an inhibitory effect on the enzyme acetylcholinesterase, which is involved in the breakdown of the neurotransmitter acetylcholine. It has also been found to have an inhibitory effect on the enzyme tyrosinase, which is involved in the synthesis of melanin.
Methyl 5-(bromomethyl)-2-fluorobenzoate has several advantages for use in laboratory experiments. It is a relatively stable compound and is not highly toxic. It is also easy to obtain and is relatively inexpensive. However, it should be handled with care, as it is highly flammable and can cause irritation of the skin and eyes.
In the future, methyl 5-(bromomethyl)-2-fluorobenzoate may be used in the synthesis of a variety of organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals. It may also be used to synthesize heterocyclic compounds, such as pyridines, quinolines, and pyrimidines. Additionally, further research may be conducted to explore its potential as an enzyme inhibitor and its effects on biochemical and physiological processes.
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Reference
[1] Pubchem: https://pubchem.ncbi.nlm.nih.gov
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