3-Fluoro-2-methylbenzyl bromide

98%

  • Product Code: 117672
  CAS:    500912-14-1
Molecular Weight: 203.06 g./mol Molecular Formula: C₈H₈BrF
EC Number: MDL Number: MFCD03788543
Melting Point: Boiling Point:
Density: Storage Condition: room temperature, dry
Product Description: 3-Fluoro-2-methylbenzyl bromide is primarily used as a versatile intermediate in organic synthesis. It plays a significant role in the development of pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs) where the introduction of fluorine atoms can enhance metabolic stability and bioavailability. This compound is also employed in the synthesis of agrochemicals, contributing to the production of herbicides and pesticides with improved efficacy. Additionally, it is utilized in material science for the preparation of specialty chemicals and polymers, where its unique structure can impart desirable properties such as thermal stability or chemical resistance. Its reactivity as a benzyl bromide makes it a valuable building block in various cross-coupling reactions, enabling the construction of complex organic molecules.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days $5,725.76
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3-Fluoro-2-methylbenzyl bromide
3-Fluoro-2-methylbenzyl bromide is primarily used as a versatile intermediate in organic synthesis. It plays a significant role in the development of pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs) where the introduction of fluorine atoms can enhance metabolic stability and bioavailability. This compound is also employed in the synthesis of agrochemicals, contributing to the production of herbicides and pesticides with improved efficacy. Additionally, it is utilized in material science for the preparation of specialty chemicals and polymers, where its unique structure can impart desirable properties such as thermal stability or chemical resistance. Its reactivity as a benzyl bromide makes it a valuable building block in various cross-coupling reactions, enabling the construction of complex organic molecules.
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