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Detail of "74896-24-5"

  • CAS Number:
  • 74896-24-5
  • Name:
  • Benzonitrile,4-amino-3,5-dimethyl-

  • Superlist Name:
  • 4-Amino-3,5-dimethylbenzonitrile
  • Molecular Structure:
  • Formula:
  • C9H10N2
  • Molecular Weight:
  • 146.19
  • Synonyms:
  • 4-Amino-3,5-dimethylbenzonitrile;NSC 128902;
  • Density:
  • 1.07 g/cm3
  • Boiling Point:
  • 322.2 °C at 760 mmHg
  • Flash Point:
  • 148.7 °C
  • Risk Codes:
  • 20/21/22-36/37/38
  • Safety:
  • 26-36/37/39 Details
  • Transport Information:
  • 3439

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CAS No.74896-24-5 4-Amino-3,5-dimethylbenzonitrile

4-AMINO-3,7-DIMETHYL-BENZONITRILE

Supplier:MolBridge LLC [ United States]

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Reference

Unusual sensitivity to the concentration of ethanol in the boron trifluoride/ethanol-catalyzed synthesis of 5,10,15,20-tetrakis(4-cyano-2,6-dimethylphenyl)porphyrin by the Lindsey method
Unusual sensitivity to the concentration of ethanol in the boron trifluoride/ethanol-catalyzed synthesis of 5,10,15,20-tetrakis(4-cyano-2,6-dimethylphenyl)porphyrin by the Lindsey method. Steiger, Beat; Anson, Fred C. (Aurthur Amos Noyes Laboratories, California Institute of Technology, Pasadena, CA 91125, USA). Journal of Heterocyclic Chemistry, 34(1), 269-272 (English) 1997 HeteroCorporation. CODEN: JHTCAD. ISSN: 0022-152X. DOCUMENT TYPE: Journal CA Section: 26 (Biomolecules and Their Synthetic Analogs) The boron trifluoride/ethanol-catalyzed condensation of 4-cyano-2,6-dimethylbenzaldehyde (I) with pyrrole by the Lindsey method to give the new, ortho-disubstituted 5,10,15,20-tetrakis(4-cyano-2,6-dimethylphenyl)porphyrin (II) was found to be highly sensitive to the concn. of ethanol. In the absence of ethanol the yield of porphyrin is only 1%. Yields can be increased to 20-25% with ethanol concns. of 0.05-0.1% (vol./vol.) but they decrease rapidly at higher concns. of ethanol. 74896-24-5 and 24596-19-8 which are cas registry numbers of substances are two of reagents here. Optimized procedures for the prepn. of both I and II are described and the newly synthesized mols. are characterized by NMR (1H and 13C), mass spectra and elemental anal. .
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