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1569293-82-8

2,2-dideuterio-2-[ethyl(phenyl)amino]acetonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1569293-82-8 Structure

  • Basic information

    1. Product Name: 2,2-dideuterio-2-[ethyl(phenyl)amino]acetonitrile
    2. Synonyms: 2,2-dideuterio-2-[ethyl(phenyl)amino]acetonitrile
    3. CAS NO:1569293-82-8
    4. Molecular Formula:
    5. Molecular Weight: 162.203
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1569293-82-8.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: 2,2-dideuterio-2-[ethyl(phenyl)amino]acetonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2-dideuterio-2-[ethyl(phenyl)amino]acetonitrile(1569293-82-8)
    11. EPA Substance Registry System: 2,2-dideuterio-2-[ethyl(phenyl)amino]acetonitrile(1569293-82-8)

  • 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: 1569293-82-8(Hazardous Substances Data)

1569293-82-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1569293-82-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,9,2,9 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1569293-82:
(9*1)+(8*5)+(7*6)+(6*9)+(5*2)+(4*9)+(3*3)+(2*8)+(1*2)=218
218 % 10 = 8
So 1569293-82-8 is a valid CAS Registry Number.

1569293-82-8Downstream Products

1569293-82-8Relevant articles and documents

Iron-catalyzed generation of α-amino nitriles from tertiary amines

Wagner, Alexander,Han, Wei,Mayer, Peter,Ofial, Armin R.

, p. 3058 - 3070 (2013)

The use of iron(II) chloride as catalyst, trimethylsilyl cyanide as source of cyanide ions, and tert-butyl hydroperoxide as oxidant enabled the conversion of aromatic, benzylic, and aliphatic tertiary amines into α-Amino nitriles under mild conditions. Chemoselective functionalization of N-CH3 to N-CH2CN was achieved in the presence of Nbenzyl and N-alkyl groups. N,N-Dialkylanilines, PhNR2, with R=Et, Bu, Bn furnished the alkyl-(aryl)aminoacetonitriles PhN(R)CH2CN as the main products accompanied by α-Amino nitriles generated by ordinary a-cyanation of the aniline PhNR2. Formation of PhN(R)CH2CN was rationalized by oxidative degradation of N,N-dialkylanilines to N-alkylanilines, their condensation with formaldehyde, generated by oxidation of the solvent methanol, and final trapping of the thus formed iminium ions by cyanide.

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