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2-(4-Fluorophenyl)-2-((4-fluorophenyl)amino)acetonitrile is a fluorinated α-aminonitrile compound synthesized via an environmentally friendly method, characterized by spectroscopic techniques (FT-IR, 1H-NMR), X-ray crystallography, and theoretical studies. Its chemical reactivity and NBO analyses have been investigated, along with molecular docking studies into the IDO enzyme, suggesting potential biological relevance. 2-(4-fluorophenyl)-2-((4-fluorophenyl)amino)acetonitrile's structural and electronic properties highlight its significance in synthetic and medicinal chemistry.

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  • 124573-72-4 Structure
  • Basic information

    1. Product Name: 2-(4-fluorophenyl)-2-((4-fluorophenyl)amino)acetonitrile
    2. Synonyms: 2-(4-fluorophenyl)-2-((4-fluorophenyl)amino)acetonitrile
    3. CAS NO:124573-72-4
    4. Molecular Formula:
    5. Molecular Weight: 244.244
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124573-72-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(4-fluorophenyl)-2-((4-fluorophenyl)amino)acetonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-fluorophenyl)-2-((4-fluorophenyl)amino)acetonitrile(124573-72-4)
    11. EPA Substance Registry System: 2-(4-fluorophenyl)-2-((4-fluorophenyl)amino)acetonitrile(124573-72-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 124573-72-4(Hazardous Substances Data)

124573-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124573-72-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,5,7 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 124573-72:
(8*1)+(7*2)+(6*4)+(5*5)+(4*7)+(3*3)+(2*7)+(1*2)=124
124 % 10 = 4
So 124573-72-4 is a valid CAS Registry Number.

124573-72-4Relevant articles and documents

Radical Rearrangement of Aryl/Alkylidene Malononitriles via Aza Michael Addition/Decynoformylation/Addition Sequence: An Access to α-Aminonitriles and α-Aminoamides

Bhoite, Shubhangi P.,Bansode, Ajay H.,Suryavanshi, Gurunath

, p. 14858 - 14865 (2020)

An efficient, safe, and environmentally friendly tertiary butyl hydrogen peroxide (TBHP)-mediated rearrangement of aryl/alkylidene malononitrile with anilines has been developed with in situ generation of HCN as the cyanide source for the synthesis of sub

Synthesis, spectroscopic characterization, X-ray analysis and theoretical studies on the spectral features (FT-IR, 1H-NMR), chemical reactivity, NBO analyses of 2-(4-fluorophenyl)-2-(4-fluorophenylamino)acetonitrile and its docking into IDO enz

Brahmachari, Goutam,Kumar, Abhishek,Srivastava, Ambrish Kumar,Gangwar, Shashi,Misra, Neeraj,Gupta, Vivek K.,Rajnikant

, p. 80967 - 80977 (2015)

A new fluorinated α-aminonitrile compound, namely, 2-(4-fluorophenyl)-2-(4-fluorophenylamino)acetonitrile (C14H10F2N2), has been synthesized following a 'green protocol' and characterized on the basis of its ele

Open-Chain Reissert Compounds: One-Pot Synthesis and Utility in Synthesis of Unsymmetrical Imides, α-Acylamino Carboxamides, Imidazolinones, and Hydantoins

Leblanc, Jean-Pierre,Gibson, Harry W.

, p. 1072 - 1077 (2007/10/02)

Acyclic Reissert compounds 2 and bis(Reissert compound)s 3-5 can be conveniently prepared in a biphasic system without isolation of the intermediate α-amino nitriles.Treatment of 2 with sodium hydride affords substituted unsymmetrical imides as 8.Oxidativ

Synthesis of Some New 3,4-Diarylsydnones

Csongar, Ch.,Mueller, I.,Slezak, H.,Klebsch, H.-J.,Tomaschewski, G.

, p. 1006 - 1014 (2007/10/02)

The synthesis of some new sydnones 4 is described.Their characteristic absorption maxima, mass spectroscopic fragmentation and C=O-valence vibrations are given.The sydnones 4 are synthezid by nitrosation of C,N-diarylglycines 3 (from strecker synthesis) a

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