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Weight236.315 g/mol
FormulaC13H20N2O2
Hydrogen Acceptors4
Hydrogen Donors1
Aromatic Rings1
Rotatable Bonds6

procaine (59-46-1)

Novocain  ·  Novocaine  ·  Procaine Hydrochloride

Score: #335 in Neuroscience , #477 in Biochemistry , #1520 in Biology , #1782 in Chemistry
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Alternate Names

  • Novocain
  • Novocaine
  • Procaine Hydrochloride
  • Anuject
  • Procaina Serra
  • Hewedolor-Procain
  • Prcaine chlorhydrate Lavoisier
  • procain-loges
  • Gerokit
  • Procain curasan
  • Rwo Procain
  • Procain Steigerwald
  • Geriocaine
  • Procain Rdler
  • Procain Jenapharm
  • Procain Braun
  • Lophakomp-Procain N
  • SMILES
    CCN(CC)CCOC(=O)C1=CC=C(C=C1)N
  • InChIKey
    MFDFERRIHVXMIY-UHFFFAOYSA-N

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Synthesis

4-aminobenzoic acid  +  2-Chlorotriethylamine (Ester from carboxilic acid(SN2))
Ethylboronic acid  +  Reactant (Chan-Lam coupling reaction)
Reactant  +  dimethyl sulfide (Corey-Kim oxidation of secondary alcohols)
Synthesis of procaine ›

Similar Compounds

2-(Dimethylamino)ethyl benzoate (2208-05-1)
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isopropyl 4-aminobenzoate (18144-43-9)
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tert-Butyl 4-aminobenzoate (18144-47-3)
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ethyl 4-(methylamino)benzoate (10541-82-9)
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ethyl 4-hydrazinylbenzoate (14685-90-6)
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Ethyl 4-dimethylaminobenzoate (10287-53-3)
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pentyl 4-aminobenzoate (13110-37-7)
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ethyl 3,4-diaminobenzoate (37466-90-3)
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heptyl 4-aminobenzoate (14309-40-1)
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ethyl 4-amino-3-methylbenzoate (40800-65-5)
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methyl 4-(methylamino)benzoate (18358-63-9)
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ethyl 4-acetamidobenzoate (5338-44-3)
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Benzyl p-aminobenzoate (19008-43-6)
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ethyl 4-amino-3-bromobenzoate (7149-03-3)
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21245-01-2 (21245-01-2)
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isopropyl 3-aminobenzoate (35005-25-5)
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