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CAS

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95309-31-2

4H-1,2,4-Triazol-4-amine, N-(1-methylethyl)-3,5-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 95309-31-2 Structure

  • Basic information

    1. Product Name: 4H-1,2,4-Triazol-4-amine, N-(1-methylethyl)-3,5-diphenyl-
    2. Synonyms:
    3. CAS NO:95309-31-2
    4. Molecular Formula: C17H18N4
    5. Molecular Weight: 278.357
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 95309-31-2.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: 4H-1,2,4-Triazol-4-amine, N-(1-methylethyl)-3,5-diphenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4H-1,2,4-Triazol-4-amine, N-(1-methylethyl)-3,5-diphenyl-(95309-31-2)
    11. EPA Substance Registry System: 4H-1,2,4-Triazol-4-amine, N-(1-methylethyl)-3,5-diphenyl-(95309-31-2)

  • 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: 95309-31-2(Hazardous Substances Data)

95309-31-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95309-31-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,3,0 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 95309-31:
(7*9)+(6*5)+(5*3)+(4*0)+(3*9)+(2*3)+(1*1)=142
142 % 10 = 2
So 95309-31-2 is a valid CAS Registry Number.

95309-31-2Downstream Products

95309-31-2Relevant articles and documents

Thermal Rearrrangement of 1-Alkyl-3,6-diaryl-1,4-dihydro-s-tetrazines to 1-Alkylamino-3,5-diaryl-1,2,4-triazoles

Hunter, Daniel,Neilson, Douglas G.

, p. 2779 - 2783 (2007/10/02)

s-Tetrazines having aryl substituents in either the 3- or 3,6-positions react readily with alkyl or aryl Grignard reagents to give 1-alkyl(or aryl)-1,4-dihydro-s-terazines.The 1-alkyl-1,4-dihydro-s-tetrazines rearrange in methanolic hydrogen chloride to 4-alkylamino-1,2,4-triazoles, but thermolyse readily to the less well known, isomeric 1-alkylamino-1,2,4-triazoles.Possible reaction pathways involving breakdown to nitrile and reactive intermediates such as 1,3-dipolar species are discussed.

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