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Weight227.735 g/mol
FormulaC12H18ClNO
Hydrogen Acceptors2
Hydrogen Donors2
Aromatic Rings1
Rotatable Bonds3

tulobuterol (41570-61-0)

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Areas of Application

Safety

Alternate Names

  • SMILES
    CC(C)(C)NCC(C1=CC=CC=C1Cl)O
  • InChIKey
    YREYLAVBNPACJM-UHFFFAOYSA-N

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Synthesis

2-amino-1-(2-chlorophenyl)ethanol  +  2-Chloro-2-methylpropane (Alkylation of primary amines)
Reactant  +  1,2-DICHLOROBENZENE (Grignard alcohol)
Reactant  +  tert-Butylamine (Reductive amination)
CHLOROBENZENE  +  Reactant (Friedel-Crafts alkylation)
Tert-butylboronic Acid  +  Reactant (Chan-Lam coupling reaction)
Synthesis of tulobuterol ›

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