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CAS 4133-35-1

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6-bromo-2-tetralone

Description:
6-Bromo-2-tetralone, with the CAS number 4133-35-1, is an organic compound characterized by its bicyclic structure, which consists of a naphthalene ring fused to a carbonyl group. This compound features a bromine atom substituted at the 6-position of the tetralone structure, influencing its reactivity and properties. It typically appears as a solid at room temperature and is soluble in organic solvents such as ethanol and dichloromethane, but has limited solubility in water due to its hydrophobic nature. The presence of the bromine atom can enhance electrophilic substitution reactions, making it a useful intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Additionally, 6-bromo-2-tetralone can undergo various chemical transformations, including reduction and substitution reactions, which are valuable in synthetic organic chemistry. Its unique structure and reactivity profile make it a compound of interest in both academic research and industrial applications.
Formula:C10H9BrO
InChI:InChI=1/C10H9BrO/c11-9-3-1-8-6-10(12)4-2-7(8)5-9/h1,3,5H,2,4,6H2
InChI key:InChIKey=BYHKDUFPSJWJDI-UHFFFAOYSA-N
SMILES:BrC=1C=C2C(CC(=O)CC2)=CC1
Synonyms:
  • 1,3-Difluoropropan-2-Ol
  • 2(1H)-Naphthalenone, 6-bromo-3,4-dihydro-
  • 6-Bromo-3,4-Dihydro-1H-Naphthalen-2-One
  • 6-Bromo-3,4-Dihydro-2(1H)-Naphthalenone
  • 6-Bromo-3,4-dihydronaphthalen-2(1H)-one
  • 6-Bromo-β-tetralone
  • 6B2T
  • 6-Bromo-2-tetralone
  • 6-BROMO-2-TETRALONE 98%
  • 6-Bromo-2-tetralone, 98 %
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