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1401198-67-1

C19H17N5O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1401198-67-1 Structure

  • Basic information

    1. Product Name: C19H17N5O
    2. Synonyms: C19H17N5O
    3. CAS NO:1401198-67-1
    4. Molecular Formula:
    5. Molecular Weight: 331.377
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1401198-67-1.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: C19H17N5O(CAS DataBase Reference)
    10. NIST Chemistry Reference: C19H17N5O(1401198-67-1)
    11. EPA Substance Registry System: C19H17N5O(1401198-67-1)

  • 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: 1401198-67-1(Hazardous Substances Data)

1401198-67-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1401198-67-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,1,1,9 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1401198-67:
(9*1)+(8*4)+(7*0)+(6*1)+(5*1)+(4*9)+(3*8)+(2*6)+(1*7)=131
131 % 10 = 1
So 1401198-67-1 is a valid CAS Registry Number.

1401198-67-1Relevant articles and documents

Noteworthy mechanistic precedence in the exclusive formation of one regioisomer in the Beckmann rearrangement of ketoximes of 4-piperidones annulated to pyrazolo-indole nucleus by organocatalyst derived from TCT and DMF

Tyagi, Ruchi,Kaur, Navjeet,Singh, Bhawani,Kishore

, p. 16 - 25 (2013)

Application of a very mild protocol to the Beckmann rearrangement of ketoximes of pyrazolo annulated oxocarbazole 5a and oxoazacarbazole 5b with the organocatalyst derived from 2,4,6-trichloro[1,3,5]triazine (TCT) and dimethylformamide (DMF) has been explored to provide a regioselective formation of the corresponding azepine 6a and 1,4-diazepine 6b respectively in good yield and purity. The mechanistic precedence for the exclusive formation of only one regioisomer has been discussed. Copyright Taylor & Francis Group, LLC.

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