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CAS

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30818-78-1

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

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  • 30818-78-1 Structure

  • Basic information

    1. Product Name: methyl 4-(4-phenyl-2H-1,2,3-triazol-2-yl)benzoate
    2. Synonyms: methyl 4-(4-phenyl-2H-1,2,3-triazol-2-yl)benzoate
    3. CAS NO:30818-78-1
    4. Molecular Formula:
    5. Molecular Weight: 279.298
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 30818-78-1.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: methyl 4-(4-phenyl-2H-1,2,3-triazol-2-yl)benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 4-(4-phenyl-2H-1,2,3-triazol-2-yl)benzoate(30818-78-1)
    11. EPA Substance Registry System: methyl 4-(4-phenyl-2H-1,2,3-triazol-2-yl)benzoate(30818-78-1)

  • 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: 30818-78-1(Hazardous Substances Data)

30818-78-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30818-78-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,8,1 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 30818-78:
(7*3)+(6*0)+(5*8)+(4*1)+(3*8)+(2*7)+(1*8)=111
111 % 10 = 1
So 30818-78-1 is a valid CAS Registry Number.

30818-78-1Downstream Products

30818-78-1Relevant articles and documents

Catalyst-Free Regioselective N2 Arylation of 1,2,3-Triazoles Using Diaryl Iodonium Salts

Roshandel, Sahar,Lunn, Maiko J.,Rasul, Golam,Muthiah Ravinson, Daniel Sylvinson,Suri, Suresh C.,Prakash, G. K. Surya

, p. 6255 - 6258 (2019)

The widespread application of 1,2,3-triazoles in pharmaceuticals has resulted in substantial interest toward developing efficient postmodification methods. Whereas there are many postmodification methods available to obtain N1-substituted 1,2,3-triazoles, developing a selective and convenient protocol to synthesize N2-aryl-1,2,3-triazoles has been challenging. We report a catalyst-free and regioselective method to access N2-aryl-1,2,3-triazoles in good to excellent yields (66-97%). This scalable postmodification protocol is effective for a wide range of substrates.

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