Product Name

  • Name

    4-Bromo-N-benzylideneaniline

  • EINECS
  • CAS No. 780-20-1
  • Article Data114
  • CAS DataBase
  • Density 1.28g/cm3
  • Solubility
  • Melting Point
  • Formula C13H10BrN
  • Boiling Point 359 °C at 760 mmHg
  • Molecular Weight 260.133
  • Flash Point 170.9 °C
  • Transport Information
  • Appearance
  • Safety
  • Risk Codes
  • Molecular Structure Molecular Structure of 780-20-1 (4-Bromo-N-benzylideneaniline)
  • Hazard Symbols
  • Synonyms Benzenamine, 4-bromo-N- (phenylmethylene)-;
  • PSA 12.36000
  • LogP 4.19970

Benzylidene-p-bromoaniline Specification

The Benzylidene-p-bromoaniline, with the CAS registry number 780-20-1, is also known as Benzenamine, 4-bromo-N- (phenylmethylene)-. This chemical's molecular formula is C13H10BrN and molecular weight is 260.1292. What's more, its IUPAC name is N-(4-Bromophenyl)-1-phenylmethanimine.

Physical properties about Benzylidene-p-bromoaniline are: (1)ACD/LogP: 3.91; (2)#of Rule of 5 Violations: 0; (3)#H bond acceptors: 1; (4)#H bond donors: 0; (5)#Freely Rotating Bonds: 2; (6)Polar Surface Area: 12.36 Å2; (7)Index of Refraction: 1.587; (8)Molar Refractivity: 67.96 cm3; (9)Molar Volume: 202.1 cm3; (10)Polarizability: 26.94×10-24cm3; (11)Surface Tension: 40.5 dyne/cm; (12)Density: 1.28 g/cm3; (13)Flash Point: 170.9 °C; (14)Enthalpy of Vaporization: 58.07 kJ/mol; (15)Boiling Point: 359 °C at 760 mmHg; (16)Vapour Pressure: 5.06E-05 mmHg at 25 °C.

Preparation of Benzylidene-p-bromoaniline: this chemical can be prepared by Benzaldehyde and 4-Bromo-aniline. This reaction needs reagents LiClO4, TMSCl and solvent Diethyl ether at temperature of 20 °C. The reaction time is 10 minutes.

Benzylidene-p-bromoaniline can be prepared by Benzaldehyde and 4-Bromo-aniline.Benzylidene-p-bromoaniline can be prepared by Benzaldehyde and 4-Bromo-aniline.Benzylidene-p-bromoaniline can be prepared by Benzaldehyde and 4-Bromo-aniline.

 

Uses of Benzylidene-p-bromoaniline: it can react with 3-Phenyl-2-thioxo-thiazolidin-4-one to give 3-[(4-Bromo-phenylamino)-phenyl-methyl]-1,3-dihydro-indol-2-one. The reaction occurs with catalysts Conc and HCl. The yield is 81 %.

Benzylidene-p-bromoaniline can react with 3-Phenyl-2-thioxo-thiazolidin-4-one to give 3-[(4-Bromo-phenylamino)-phenyl-methyl]-1,3-dihydro-indol-2-one.Benzylidene-p-bromoaniline can react with 3-Phenyl-2-thioxo-thiazolidin-4-one to give 3-[(4-Bromo-phenylamino)-phenyl-methyl]-1,3-dihydro-indol-2-one.Benzylidene-p-bromoaniline can react with 3-Phenyl-2-thioxo-thiazolidin-4-one to give 3-[(4-Bromo-phenylamino)-phenyl-methyl]-1,3-dihydro-indol-2-one.

 

You can still convert the following datas into molecular structure:
(1) SMILES: Brc2ccc(/N=C/c1ccccc1)cc2
(2) InChI: InChI=1/C13H10BrN/c14-12-6-8-13(9-7-12)15-10-11-4-2-1-3-5-11/h1-10H/b15-10+
(3) InChIKey: DJGDQBWKJYPZEF-XNTDXEJSBM

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