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CAS

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101794-35-8

N,N'-dibenzylpyrimidine-4,6-diamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 101794-35-8 Structure

  • Basic information

    1. Product Name: N,N'-dibenzylpyrimidine-4,6-diamine
    2. Synonyms: N,N'-dibenzylpyrimidine-4,6-diamine
    3. CAS NO:101794-35-8
    4. Molecular Formula:
    5. Molecular Weight: 290.368
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 101794-35-8.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: N,N'-dibenzylpyrimidine-4,6-diamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N'-dibenzylpyrimidine-4,6-diamine(101794-35-8)
    11. EPA Substance Registry System: N,N'-dibenzylpyrimidine-4,6-diamine(101794-35-8)

  • 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: 101794-35-8(Hazardous Substances Data)

101794-35-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101794-35-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,7,9 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 101794-35:
(8*1)+(7*0)+(6*1)+(5*7)+(4*9)+(3*4)+(2*3)+(1*5)=108
108 % 10 = 8
So 101794-35-8 is a valid CAS Registry Number.

101794-35-8Relevant articles and documents

A method for the reductive scission of heterocyclic thioethers

Graham, Thomas H.,Liu, Wensheng,Shen, Dong-Ming

supporting information; experimental part, p. 6232 - 6235 (2012/01/03)

A mild, chemoselective, and generally high-yielding method for the reductive scission of heterocyclic thioethers is described. Suitable heterocycles have a thioether substituent at the 2-position relative to a ring heteroatom. The convenient and straightforward method is demonstrated with reactants which are not compatible with the standard Raney nickel conditions such as sulfides, sulfones, and thiophenes. In addition, benzyl esters, benzyl amides, and benzyl carbamates are tolerated by the reductive reaction conditions.

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