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1224437-17-5

C17H19N3O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1224437-17-5 Structure

  • Basic information

    1. Product Name: C17H19N3O2
    2. Synonyms:
    3. CAS NO:1224437-17-5
    4. Molecular Formula:
    5. Molecular Weight: 297.357
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1224437-17-5.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: C17H19N3O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C17H19N3O2(1224437-17-5)
    11. EPA Substance Registry System: C17H19N3O2(1224437-17-5)

  • 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: 1224437-17-5(Hazardous Substances Data)

1224437-17-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1224437-17-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,4,4,3 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1224437-17:
(9*1)+(8*2)+(7*2)+(6*4)+(5*4)+(4*3)+(3*7)+(2*1)+(1*7)=125
125 % 10 = 5
So 1224437-17-5 is a valid CAS Registry Number.

1224437-17-5Upstream product

1224437-17-5Downstream Products

1224437-17-5Relevant articles and documents

Synthesis of 5-arylpyrrolo[2,1-c][1,4]benzodiazepines under mild cyclodehydration conditions

Legerén, Loreto,Domínguez, Domingo

experimental part, p. 2718 - 2722 (2010/05/02)

The efficiency of a cyclodehydration reaction leading to benzodiazepinones is markedly improved by N-methylation of the amide link connecting the nucleophile and the electrophile, which is attributed to its favouring both the more reactive E-rotamer and the exit of the leaving group.

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