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84199-02-0

N1,N1-dibenzyl-N2-methylethane-1,2-diamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 84199-02-0 Structure

  • Basic information

    1. Product Name: N1,N1-dibenzyl-N2-methylethane-1,2-diamine
    2. Synonyms: N1,N1-dibenzyl-N2-methylethane-1,2-diamine
    3. CAS NO:84199-02-0
    4. Molecular Formula:
    5. Molecular Weight: 254.375
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 84199-02-0.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: N1,N1-dibenzyl-N2-methylethane-1,2-diamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N1,N1-dibenzyl-N2-methylethane-1,2-diamine(84199-02-0)
    11. EPA Substance Registry System: N1,N1-dibenzyl-N2-methylethane-1,2-diamine(84199-02-0)

  • 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: 84199-02-0(Hazardous Substances Data)

84199-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84199-02-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,1,9 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 84199-02:
(7*8)+(6*4)+(5*1)+(4*9)+(3*9)+(2*0)+(1*2)=150
150 % 10 = 0
So 84199-02-0 is a valid CAS Registry Number.

84199-02-0Relevant articles and documents

Chiral ureas and thioureas supported on polystyrene for enantioselective aza-Henry reactions under solvent-free conditions

Pedrosa, Rafael,Andrés, José M.,ávila, Deisy P.,Ceballos, Miriam,Pindado, Rodrigo

, p. 2217 - 2225 (2015)

Novel bifunctional ureas and thioureas immobilized on sulfonylpolystyrene have been prepared as recoverable and reusable organocatalysts and have been used in the stereoselective aza-Henry reaction under solvent-free conditions. The activity and stereoselection of the catalysts are dependent on the length of the tether bridging the active site and the polymer, the catalyst derived from 1,6-hexane diamine being the best one. It has also been demonstrated that the supported catalysts are more effective than the homologous soluble catalysts.

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