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1586017-53-9

C15H13N5O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1586017-53-9 Structure

  • Basic information

    1. Product Name: C15H13N5O
    2. Synonyms:
    3. CAS NO:1586017-53-9
    4. Molecular Formula:
    5. Molecular Weight: 279.301
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1586017-53-9.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: C15H13N5O(CAS DataBase Reference)
    10. NIST Chemistry Reference: C15H13N5O(1586017-53-9)
    11. EPA Substance Registry System: C15H13N5O(1586017-53-9)

  • 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: 1586017-53-9(Hazardous Substances Data)

1586017-53-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1586017-53-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,6,0,1 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1586017-53:
(9*1)+(8*5)+(7*8)+(6*6)+(5*0)+(4*1)+(3*7)+(2*5)+(1*3)=179
179 % 10 = 9
So 1586017-53-9 is a valid CAS Registry Number.

1586017-53-9Downstream Products

1586017-53-9Relevant articles and documents

Reaction of 2-aryl-4-cyano-1,3-oxazole-5-sulfonyl chlorides with 5-amino-1h-pyrazoles and 5-amino-1h-1,2,4-triazole

Kornienko,Pil'O,Kozachenko,Prokopenko,Rusanov,Brovarets

, p. 76 - 86 (2014)

The reaction of 2-aryl-4-cyano-1,3-oxazole-5-sulfonyl chlorides with 5-amino-3-R-1H-pyrazoles and 5-amino-1H-1,2,4-triazole gave 5-[(3-R-5-amino-1H- pyrazol-1-yl)sulfonyl]-2-aryl-1,3-oxazole-4-carbo- nitriles and 5-[(5-amino-1H-1,2,4-triazol-1-yl)sulfonyl]-2-aryl-1,3-oxazole-4-carbonitriles. The action of sodium hydride on these carbonitriles leads to the elimination of sulfur dioxide and cyclocondensation to give new heterocyclic systems, namely, [1,3]oxazolo[5,4-d]pyrazolo[1,5-a]-pyrimidine and [1,3]oxazolo[5,4-d][1,2,4] triazolo[1,5-a]pyrimidine.

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