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CAS

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15296-47-6

N-p-tolyl-formimidic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 15296-47-6 Structure

  • Basic information

    1. Product Name: N-p-tolyl-formimidic acid ethyl ester
    2. Synonyms: N-p-tolyl-formimidic acid ethyl ester
    3. CAS NO:15296-47-6
    4. Molecular Formula:
    5. Molecular Weight: 163.219
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 15296-47-6.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-p-tolyl-formimidic acid ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-p-tolyl-formimidic acid ethyl ester(15296-47-6)
    11. EPA Substance Registry System: N-p-tolyl-formimidic acid ethyl ester(15296-47-6)

  • 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: 15296-47-6(Hazardous Substances Data)

15296-47-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15296-47-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,9 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15296-47:
(7*1)+(6*5)+(5*2)+(4*9)+(3*6)+(2*4)+(1*7)=116
116 % 10 = 6
So 15296-47-6 is a valid CAS Registry Number.

15296-47-6Relevant articles and documents

Multicomponent synthesis of 1-aryl 1,2,4-triazoles

Tam, Annie,Armstrong, Ian S.,La Cruz, Thomas E.

supporting information, p. 3586 - 3589 (2013/08/23)

A multicomponent (single reactor) process for the synthesis of 1-aryl 1,2,4-triazoles was explored and developed. This transformation prepared the 1,2,4-triazole directly from anilines, amino pyridines, and pyrimidines. The reaction scope was explored with 21 different substrates, and the position of the nitrogen atoms in the newly formed ring was established by 15N labeling and NMR spectroscopy.

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