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N-(3-(Phenylamino)allylidene)aniline hydrochloride

  • CAS No. 28140-60-5

  • Cat. No. CS-0188271
  • Purity≥95%
  • MDL No.MFCD00467013

*For research and further manufacturing use only, not for direct human use.

N-(3-(Phenylamino)allylidene)aniline hydrochloride|CS-0188271

Structure of 28140-60-5

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General Information

  • CAS No. 28140-60-5
  • Cat. No. CS-0188271
  • Purity ≥95%
  • MDL No. MFCD00467013
  • Storage Store at room temperature, keep dry and cool
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₅H₁₅ClN₂
  • Molecular Weight 258.75
  • Synonym(s) Malonaldehyde Bis(phenylimine) Hydrochloride
  • SMILES C1(N/C=C/C=N/C2=CC=CC=C2)=CC=CC=C1.Cl

Description

N-(3-(Phenylamino)allylidene)aniline hydrochloride features a conjugated imine system with an electron-rich phenylamino group, enabling efficient π-delocalization and enhanced stability. This bench-stable salt serves as a key intermediate in the synthesis of functionalized heterocycles and advanced organic semiconductors.

Application

N-(3-(Phenylamino)allylidene)aniline hydrochloride serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted indoles and related scaffolds via cyclization reactions. The imine functionality facilitates electrophilic substitution and condensation processes under mild conditions, while the hydrochloride salt enhances solubility and stability for bench-scale handling. Its robust functional group tolerance supports integration into multi-step synthetic sequences.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302
Precautionary Statements : P264-P270-P330-P501

Quality Control

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Computational Chemistry Data

  • TPSA   24.39
  • LogP   4.4365
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   4

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