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CAS

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192631-79-1

4,6-Pyrimidinediamine, N-cyclohexyl-5-nitro-2-phenyl-N'-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 192631-79-1 Structure

  • Basic information

    1. Product Name: 4,6-Pyrimidinediamine, N-cyclohexyl-5-nitro-2-phenyl-N'-(phenylmethyl)-
    2. Synonyms:
    3. CAS NO:192631-79-1
    4. Molecular Formula: C23H25N5O2
    5. Molecular Weight: 403.484
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 192631-79-1.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: 4,6-Pyrimidinediamine, N-cyclohexyl-5-nitro-2-phenyl-N'-(phenylmethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4,6-Pyrimidinediamine, N-cyclohexyl-5-nitro-2-phenyl-N'-(phenylmethyl)-(192631-79-1)
    11. EPA Substance Registry System: 4,6-Pyrimidinediamine, N-cyclohexyl-5-nitro-2-phenyl-N'-(phenylmethyl)-(192631-79-1)

  • 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: 192631-79-1(Hazardous Substances Data)

192631-79-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 192631-79-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,6,3 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 192631-79:
(8*1)+(7*9)+(6*2)+(5*6)+(4*3)+(3*1)+(2*7)+(1*9)=151
151 % 10 = 1
So 192631-79-1 is a valid CAS Registry Number.

192631-79-1Downstream Products

192631-79-1Relevant articles and documents

Synthesis of 4,6-disubstituted- and 4,5,6-trisubstituted-2-phenyl- pyrimidines and their affinity towards A1 adenosine receptors

Biagi,Giorgi,Livi,Scartoni,Lucacchini

, p. 61 - 65 (2007/10/03)

Synthesis and assay of title compounds are reported. The results can support our hypothesis about the possibility that molecules characterized by great flexibility, as the title 2-phenyl-4,5,6-triaminopyrimidines, can better interact with the receptor sites compared with rigid molecules as 2,6,9-trisubstituted 8-azaadenines. Relatively low activity shown by pyrimidine derivatives demonstrated the importance of the bicyclic aromatic system in 8-azaadenines and adenines to give a favourable interaction between a hexogenous molecule and the A1 adenosine receptors.

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