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N~1~,N~2~-dimethyl-N'~1~,N'~2~-bis(4-methylphenyl)-N~1~,N~2~-diphenylethanediimidamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 167966-97-4 Structure
  • Basic information

    1. Product Name: N~1~,N~2~-dimethyl-N'~1~,N'~2~-bis(4-methylphenyl)-N~1~,N~2~-diphenylethanediimidamide
    2. Synonyms: N~1~,N~2~-dimethyl-N'~1~,N'~2~-bis(4-methylphenyl)-N~1~,N~2~-diphenylethanediimidamide
    3. CAS NO:167966-97-4
    4. Molecular Formula: C30H30N4
    5. Molecular Weight: 446.586
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 167966-97-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N~1~,N~2~-dimethyl-N'~1~,N'~2~-bis(4-methylphenyl)-N~1~,N~2~-diphenylethanediimidamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N~1~,N~2~-dimethyl-N'~1~,N'~2~-bis(4-methylphenyl)-N~1~,N~2~-diphenylethanediimidamide(167966-97-4)
    11. EPA Substance Registry System: N~1~,N~2~-dimethyl-N'~1~,N'~2~-bis(4-methylphenyl)-N~1~,N~2~-diphenylethanediimidamide(167966-97-4)
  • 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: 167966-97-4(Hazardous Substances Data)

167966-97-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 167966-97-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,9,6 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 167966-97:
(8*1)+(7*6)+(6*7)+(5*9)+(4*6)+(3*6)+(2*9)+(1*7)=204
204 % 10 = 4
So 167966-97-4 is a valid CAS Registry Number.

167966-97-4Downstream Products

167966-97-4Relevant articles and documents

On the Aminolysis of Bis-Imidoylchlorides of Oxalic Acid. Part I. Reaction with Aromatic and Aliphatic Amines

Lindauer, Dirk,Beckert, Rainer,Doering, Manfred,Fehling, Peer,Goerls, Helmar

, p. 143 - 152 (2007/10/02)

The reaction between bis-imidoylchlorides 2 derived from oxalic acid several aromatic and aliphatic amines was investigated.While primary aromatic amines need a thermical activation by refluxing, primary aliphatic amines give mainly at room temperature the amidines 3 in moderatly up to good yields.Proceeding from enantiomeric pure amines e.g. (R)- or (S)-1-phenylethylamine the new homochiral axalic amidines 3y and 3z with C2-symmetry were obtained.Several secondary amines react with the bis-imidoylchloride 2a to give via intramolecular cycloacylation derivatives of isatine.The new synthesized amidines 3 perform systems with a strong molecular dynamic like prototropic and E/Z-interconversion.All new compounds described were characterized by elemental analysis and spectroscopic methods.

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