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1417450-08-8

3-phenyl-1-(tetrahydro-2H-pyran-2-yl)-1H-1,2,4-triazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1417450-08-8 Structure

  • Basic information

    1. Product Name: 3-phenyl-1-(tetrahydro-2H-pyran-2-yl)-1H-1,2,4-triazole
    2. Synonyms: 3-phenyl-1-(tetrahydro-2H-pyran-2-yl)-1H-1,2,4-triazole
    3. CAS NO:1417450-08-8
    4. Molecular Formula:
    5. Molecular Weight: 229.282
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1417450-08-8.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: 3-phenyl-1-(tetrahydro-2H-pyran-2-yl)-1H-1,2,4-triazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-phenyl-1-(tetrahydro-2H-pyran-2-yl)-1H-1,2,4-triazole(1417450-08-8)
    11. EPA Substance Registry System: 3-phenyl-1-(tetrahydro-2H-pyran-2-yl)-1H-1,2,4-triazole(1417450-08-8)

  • 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: 1417450-08-8(Hazardous Substances Data)

1417450-08-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1417450-08-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,7,4,5 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1417450-08:
(9*1)+(8*4)+(7*1)+(6*7)+(5*4)+(4*5)+(3*0)+(2*0)+(1*8)=138
138 % 10 = 8
So 1417450-08-8 is a valid CAS Registry Number.

1417450-08-8Relevant articles and documents

C-H bonds as ubiquitous functionality: Preparation of multiple regioisomers of arylated 1,2,4-triazoles via C-H arylation

Joo, Jung Min,Guo, Pengfei,Sames, Dalibor

, p. 738 - 743 (2013/02/25)

We describe a general approach for the synthesis of complex aryl 1,2,4-triazoles. The electronic character of the C-H bonds and the triazole ring allows for the regioselective C-H arylation of 1-alkyl- and 4-alkyltriazoles under catalytic conditions. We have also developed the SEM and THP switch as well as trans-N-alkylation, which enable sequential arylation of the triazole ring to prepare 3,5-diaryltriazoles. This new strategy provides rapid access to a variety of arylated 1,2,4-triazoles and well complements existing cyclization methods.

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