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4-[[(4-Fluorophenyl)imino]methyl]-phenol

  • CAS：3382-63-6
  • purity：99%
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4-[[(4-Fluorophenyl)imino]methyl]-phenol GMP Manufacturer Global Trade 3382-63-6 with Fast Delivery

  • Molecular Formula: C13H10FNO
  • Molecular Weight: 215.227
  • Vapor Pressure: 0mmHg at 25°C 
  • Melting Point: 179.0 to 183.0 °C 
  • Refractive Index: 1.558 
  • Boiling Point: 370.9 °C at 760 mmHg 
  • PKA: 8.56±0.15(Predicted) 
  • Flash Point: 178.1 °C 
  • PSA： 32.59000 
  • Density: 1.13 g/cm3 
  • LogP: 3.28190 

4-[[(4-Fluorophenyl)imino]methyl]-phenol(Cas 3382-63-6) Usage

InChI:InChI=1/C13H10FNO/c14-11-3-5-12(6-4-11)15-9-10-1-7-13(16)8-2-10/h1-9,16H/b15-9+

3382-63-6 Relevant articles

A New Pathway for Protein Haptenation by β-Lactams

Pérez-Ruíz, Raúl,Lence, Emilio,Andreu, Inmaculada,Limones-Herrero, Daniel,González-Bello, Concepción,Miranda, Miguel A.,Jiménez, M. Consuelo

, p. 13986 - 13994 (2017)

The covalent binding of β-lactams to pro...

Mesomorphic properties and X-ray diffraction studies of 4-alkanoyloxybenzylidene-4′-fluoroaniline

Ha, Sie-Tiong,Lee, Teck-Leong,Lee, Siew-Ling,Yeap, Guan-Yeow,Lin, Hong-Cheu,Ito, Masato M.

, p. 7737 - 7740 (2014)

A new homologous series of Schiff base e...

Additional effect of para-hydroxyl on the reduction potentials of the N-benzylidenebenzenamines

Cao, Chao-Tun,Zhou, Wei,Cao, Chenzhong

, (2019/12/27)

The reduction potential ERed of disubsti...

Effect of substituents on the UV spectra of supermolecular system: Silver nanoparticles with bi-aryl Schiff bases containing hydroxyl

Cao, Chao-Tun,Cheng, Shimao,Zhang, Jingyuan,Cao, Chenzhong

, (2018/11/25)

Effect of substituents on the ultraviole...

Iron-Catalyzed Nitrene Transfer Reaction of 4-Hydroxystilbenes with Aryl Azides: Synthesis of Imines via C=C Bond Cleavage

Peng, Yi,Fan, Yan-Hui,Li, Si-Yuan,Li, Bin,Xue, Jing,Deng, Qing-Hai

supporting information, p. 8389 - 8394 (2019/10/16)

C=C bond breaking to access the C=N bond...

Production method of Ezetimibe intermediate

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Paragraph 0029; 0030; 0031, (2017/08/29)

The invention discloses a two-stage thre...

3382-63-6 Process route

4-hydroxy-benzaldehyde
123-08-0,65581-83-1

4-hydroxy-benzaldehyde

4-fluoroaniline
371-40-4

4-fluoroaniline

N-(4-hydroxybenzylidene)-4-fluorobenzenamine
3382-63-6,942485-62-3

N-(4-hydroxybenzylidene)-4-fluorobenzenamine

Conditions
Conditions Yield
In water; at 20 - 85 ℃; for 5.5h; Large scale;
97.5%
In methanol; at 20 - 30 ℃; Large scale;
90%
In isopropyl alcohol; at 50 ℃; for 1h;
88%
In ethanol;
84%
In isopropyl alcohol; at 50 ℃; for 1h;
80%
In ethanol; for 4h; Reflux;
In methanol; for 3h; Reflux;
With acetic acid; In dichloromethane; at 20 ℃;
In ethanol; Reflux;
In ethanol; at 20 ℃; for 3.25h;
In ethanol; Reflux;
In ethanol; at 20 ℃; for 0.5h;
p-azidofluorobenzene
3296-02-4

p-azidofluorobenzene

trans-4-Hydroxystilbene
6554-98-9

trans-4-Hydroxystilbene

N-benzylidene-4-fluoroaniline
331-98-6,83306-62-1,83306-65-4

N-benzylidene-4-fluoroaniline

N-(4-hydroxybenzylidene)-4-fluorobenzenamine
3382-63-6,942485-62-3

N-(4-hydroxybenzylidene)-4-fluorobenzenamine

Conditions
Conditions Yield
With iron(II) chloride; In acetonitrile; at 100 ℃; Sealed tube; Inert atmosphere;

3382-63-6 Upstream products

  • 123-08-0
    123-08-0

    4-hydroxy-benzaldehyde

  • 371-40-4
    371-40-4

    4-fluoroaniline

  • 163222-33-1
    163222-33-1

    ezetemibe

  • 3296-02-4
    3296-02-4

    p-azidofluorobenzene

3382-63-6 Downstream products

  • 1159183-26-2
    1159183-26-2

    N-(4-trityloxybenzylidene)-4-fluoroaniline

  • 954109-25-2
    954109-25-2

    (S)-3-{(R)-2-[(S)-(4-fluorophenylamino)-(4-hydroxyphenyl)methyl]-4-[2-(4-fluorophenyl)-[1,3]-dioxolan-2-yl]butyryl}-4-phenyloxazolidin-2-one

  • 1185883-42-4
    1185883-42-4

    C41 H34 F2 N2 O7

  • 1159183-27-3
    1159183-27-3

    benzyl-[4-(4-fluorophenyliminomethyl)phenyl]-carbonate

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