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1360813-58-6

C17H17N3O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1360813-58-6 Structure

  • Basic information

    1. Product Name: C17H17N3O2
    2. Synonyms: C17H17N3O2
    3. CAS NO:1360813-58-6
    4. Molecular Formula:
    5. Molecular Weight: 295.341
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1360813-58-6.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: C17H17N3O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C17H17N3O2(1360813-58-6)
    11. EPA Substance Registry System: C17H17N3O2(1360813-58-6)

  • 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: 1360813-58-6(Hazardous Substances Data)

1360813-58-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1360813-58-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,0,8,1 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1360813-58:
(9*1)+(8*3)+(7*6)+(6*0)+(5*8)+(4*1)+(3*3)+(2*5)+(1*8)=146
146 % 10 = 6
So 1360813-58-6 is a valid CAS Registry Number.

1360813-58-6Downstream Products

1360813-58-6Relevant articles and documents

A new convenient synthesis of 5-aryl-2-(arylamino)-1,3,4-oxadiazole derivatives

Kumar, Sanjeev

, p. 216 - 220 (2012/08/29)

Electrical energy offers numerous benefits for conducting a synthesis, including increased reaction rates, yield enhancements and cleaner chemistries. 5-Aryl-2-(arylamino)-1,3,4-oxadiazoles were synthesized directly from acylthiosemicarbazide on the plati

A new convenient synthesis of 5-aryl-2-(arylamino)-1,3,4-oxadiazole derivatives

Kumar, Sanjeev

, p. 216 - 220 (2015/03/03)

Electrical energy offers numerous benefits for conducting a synthesis, including increased reaction rates, yield enhancements and cleaner chemistries. 5-Aryl-2-(arylamino)-1,3,4-oxadiazoles were synthesised directly from acylthiosemicarbazide on the platinum electrode under controlled potential electrolysis in an undivided cell assembly in acetonitrile.

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