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808758-81-8

808758-81-8 Structure

808758-81-8 Structure
IdentificationBack Directory
[Name]

4-(bis(4-iodophenyl)aMino)benzaldehyde
[CAS]

808758-81-8
[Synonyms]

4-(bis(4-iodophenyl)aMino)benzaldehyde
Benzaldehyde, 4-[bis(4-iodophenyl)amino]-
4-[Bis(4-iodophenyl)amino]benzaldehyde >
4-(4-iodo-N-(4-iodophenyl)anilino)benzaldehyde
4-(bis(4-iodophenyl)aMino)benzaldehyde USP/EP/BP
[Molecular Formula]

C19H13I2NO
[MDL Number]

MFCD20259247
[MOL File]

808758-81-8.mol
[Molecular Weight]

525.122
Chemical PropertiesBack Directory
[Melting point ]

139.0 to 143.0 °C
[Boiling point ]

560.6±45.0 °C(Predicted)
[density ]

1.899±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[form ]

powder to crystal
[pka]

-6.96±0.50(Predicted)
[color ]

Light yellow to Yellow to Orange
[InChI]

InChI=1S/C19H13I2NO/c20-15-3-9-18(10-4-15)22(19-11-5-16(21)6-12-19)17-7-1-14(13-23)2-8-17/h1-13H
[InChIKey]

HIUBJHKIRVFTOM-UHFFFAOYSA-N
[SMILES]

C(=O)C1=CC=C(N(C2=CC=C(I)C=C2)C2=CC=C(I)C=C2)C=C1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2922.39.5000
Spectrum DetailBack Directory
[Spectrum Detail]

4-(bis(4-iodophenyl)aMino)benzaldehyde(808758-81-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-(N,N-Diphenylamino)benzaldehyde

4181-05-9

4-(bis(4-iodophenyl)aMino)benzaldehyde

808758-81-8

4-(Bis(4-iodophenyl)amino)benzaldehyde (3) was synthesized as follows: in a 100 mL two-necked flask equipped with a nitrogen inlet, a magnetic stirrer and a condenser, 4-(diphenylamino)benzaldehyde (2) (3.8 g, 13.9 mmol), potassium iodide (3.0 g, 18.1 mmol), acetic acid (45.0 mL), and deionized water (5.0 mL ). The reaction mixture was heated to 80 °C and potassium iodate (2.98 g, 13.9 mmol) was added quickly. The resulting mixture was stirred continuously at 80 °C for 5 hours. Upon completion of the reaction, the solution was cooled to room temperature and slowly poured into ice water with stirring. The resulting yellow precipitate was collected by filtration and washed with 5% mass fraction NaHSO3 solution (40.0 mL). After filtration, the target product 4-(bis(4-iodophenyl)amino)benzaldehyde (3) was obtained as a yellow solid (7.0 g, 13.4 mmol, 96% yield). The 1H NMR spectrum of the product was in agreement with literature reports (Ning et al., 2007).

[References]

[1] Journal of Polymer Science, Part A: Polymer Chemistry, 2010, vol. 48, # 15, p. 3417 - 3430
[2] Chemical Papers, 2015, vol. 70, # 2, p. 218 - 230
[3] Tetrahedron Letters, 2007, vol. 48, # 33, p. 5877 - 5881
[4] Tetrahedron, 2008, vol. 64, # 24, p. 5736 - 5742
[5] New Journal of Chemistry, 2009, vol. 33, # 10, p. 2120 - 2127
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