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Atomfair 1,3-Dibromo-5-tert-butylbenzene C10H12Br2

Description 1,3-Dibromo-5-tert-butylbenzene (CAS No. 129316-09-2) is a high-purity brominated aromatic compound with the molecular formula C10H12Br2. This specialty chemical features a tert-butyl group at the 5-position and bromine substituents at the 1- and 3-positions of the benzene ring, offering unique steric and electronic properties for advanced synthetic applications. With a molecular weight of 292.01 g/mol, it is supplied as a crystalline solid with exceptional purity (>98%) suitable for demanding research and industrial processes. The compound’s robust structure makes it valuable as a building block in organic synthesis, particularly in the preparation of ligands, pharmaceuticals, and functional materials. Proper handling requires…

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Description

Description

1,3-Dibromo-5-tert-butylbenzene (CAS No. 129316-09-2) is a high-purity brominated aromatic compound with the molecular formula C10H12Br2. This specialty chemical features a tert-butyl group at the 5-position and bromine substituents at the 1- and 3-positions of the benzene ring, offering unique steric and electronic properties for advanced synthetic applications. With a molecular weight of 292.01 g/mol, it is supplied as a crystalline solid with exceptional purity (>98%) suitable for demanding research and industrial processes. The compound’s robust structure makes it valuable as a building block in organic synthesis, particularly in the preparation of ligands, pharmaceuticals, and functional materials. Proper handling requires PPE due to potential irritant properties.

  • CAS No: 129316-09-2
  • Molecular Formula: C10H12Br2
  • Molecular Weight: 292.01
  • Exact Mass: 291.92853
  • Monoisotopic Mass: 289.93058
  • IUPAC Name: 1,3-dibromo-5-tert-butylbenzene
  • SMILES: CC(C)(C)C1=CC(=CC(=C1)Br)Br
  • Synonyms: 1,3-dibromo-5-tert-butylbenzene, 129316-09-2, DTXSID50375598, DTXCID50326626, 690-468-8

Application

1,3-Dibromo-5-tert-butylbenzene serves as a key intermediate in the synthesis of sterically hindered ligands for transition metal catalysis. Researchers utilize its bromine substituents for Suzuki-Miyaura cross-coupling reactions to construct complex biaryl systems. The tert-butyl group enhances solubility in organic solvents while influencing molecular packing in material science applications. It is also employed in pharmaceutical research for developing novel active ingredients.

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