Atomfair Benzene, 1-bromo-3,5-dimethyl- 5-Bromo-m-xylene C8H9Br

Description 1-Bromo-3,5-dimethylbenzene (CAS No. 40032-73-3), also known as 5-Bromo-m-xylene, is a high-purity aromatic compound with the molecular formula C8H9Br. This halogenated derivative of m-xylene features a bromine substituent at the 1-position and methyl groups at the 3- and 5-positions, offering unique reactivity for electrophilic substitution and coupling reactions. Ideal for pharmaceutical intermediates, agrochemical synthesis, and advanced material research, this compound is rigorously tested to meet analytical standards (GC/HPLC ??98%). Packaged under inert gas to ensure stability, it is available in quantities from grams to bulk orders with custom purity options upon request. Suitable for use in Suzuki-Miyaura cross-coupling, lithiation, and…

Description

Description

1-Bromo-3,5-dimethylbenzene (CAS No. 40032-73-3), also known as 5-Bromo-m-xylene, is a high-purity aromatic compound with the molecular formula C8H9Br. This halogenated derivative of m-xylene features a bromine substituent at the 1-position and methyl groups at the 3- and 5-positions, offering unique reactivity for electrophilic substitution and coupling reactions. Ideal for pharmaceutical intermediates, agrochemical synthesis, and advanced material research, this compound is rigorously tested to meet analytical standards (GC/HPLC ??98%). Packaged under inert gas to ensure stability, it is available in quantities from grams to bulk orders with custom purity options upon request. Suitable for use in Suzuki-Miyaura cross-coupling, lithiation, and as a building block in organic synthesis.

  • CAS No: 40032-73-3
  • Molecular Formula: C8H9Br
  • Molecular Weight: 185.06
  • Exact Mass: 183.98876
  • Monoisotopic Mass: 183.98876
  • IUPAC Name: 1-bromo-3,5-dimethylbenzene
  • SMILES: CC1=CC(=CC(=C1)Br)C
  • Synonyms: 5-Bromo-m-xylene, 556-96-7, Benzene, 1-bromo-3,5-dimethyl-, DTXSID00204142, DTXCID00126633

Application

1-Bromo-3,5-dimethylbenzene is widely used as a versatile intermediate in organic synthesis, particularly in palladium-catalyzed cross-coupling reactions (e.g., Suzuki, Heck) to construct biaryl scaffolds. Its electron-rich aromatic system makes it valuable for synthesizing ligands, agrochemicals, and pharmaceutical candidates. Researchers also employ it in material science for designing liquid crystals or polymers with tailored properties.

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