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CAS 132392-28-0

:

2-BROMO-1-(5,5,8,8-TETRAMETHYL-5,6,7,8-TETRAHYDRONAPHTHALEN-2-YL)ETHAN-1-ONE

Description:
2-Bromo-1-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)ethan-1-one, with CAS number 132392-28-0, is an organic compound characterized by its complex structure, which includes a bromine atom and a ketone functional group. This compound features a tetrahydronaphthalene moiety, which contributes to its hydrophobic nature and potential applications in organic synthesis and medicinal chemistry. The presence of the bromine atom enhances its reactivity, making it a useful intermediate in various chemical reactions, such as nucleophilic substitutions. The bulky tetramethyl substituents provide steric hindrance, influencing the compound's reactivity and stability. Additionally, the compound's unique structure may impart specific biological activities, making it of interest in pharmaceutical research. Its physical properties, such as melting point, boiling point, and solubility, would typically be determined through experimental methods, as they can vary based on purity and environmental conditions. Overall, this compound exemplifies the intricate interplay between structure and reactivity in organic chemistry.
Formula:C16H21BrO
InChI:InChI=1/C16H21BrO/c1-15(2)7-8-16(3,4)13-9-11(14(18)10-17)5-6-12(13)15/h5-6,9H,7-8,10H2,1-4H3
SMILES:CC1(C)CCC(C)(C)c2cc(ccc12)C(=O)CBr
Synonyms:
  • 6-(Bromoacetyl)-1,2,3,4-Tetrahydro-1,1,4,4-Tetramethylnaphthalene
  • 2-Bromo-1-(5,5,8,8-tetramethyl-5,6,7,8-tet
  • 6-(Bromoacetyl)-1,2,3,4-Tetrahydro-1,1,4,4-Tetramethylnaphthalene, Tech.
  • 2-Bromo-1-(5,5,8,8-Tetramethyl-5,6,7,8-Tetrahydronaphthalen-2-Yl)Ethanone
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