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CAS

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69063-05-4

8-chloro-1H-1,4-benzodiazepin-5-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 69063-05-4 Structure

  • Basic information

    1. Product Name: 8-chloro-1H-1,4-benzodiazepin-5-one
    2. Synonyms:
    3. CAS NO:69063-05-4
    4. Molecular Formula:
    5. Molecular Weight: 194.62
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 69063-05-4.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: 8-chloro-1H-1,4-benzodiazepin-5-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 8-chloro-1H-1,4-benzodiazepin-5-one(69063-05-4)
    11. EPA Substance Registry System: 8-chloro-1H-1,4-benzodiazepin-5-one(69063-05-4)

  • 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: 69063-05-4(Hazardous Substances Data)

69063-05-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69063-05-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,0,6 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 69063-05:
(7*6)+(6*9)+(5*0)+(4*6)+(3*3)+(2*0)+(1*5)=134
134 % 10 = 4
So 69063-05-4 is a valid CAS Registry Number.

69063-05-4Downstream Products

69063-05-4Relevant articles and documents

Photolysis of Quinolyl and Isoquinolyl Azides in the Presence of Methoxide Ions. Synthesis of Benzodiazepines and Pyridoazepines

Hollywood, Frank,Khan, Zafar U.,Scriven, Eric F. V.,Smalley, Robert K.,Suschitzky, Hans,et al.

, p. 431 - 433 (2007/10/02)

Photolysis of the title compounds in the presence of methoxide provides a convenient preparation of the corresponding methoxy-substituted bicyclic azepines and benzodiazepines in one step from readily available starting materials.Moreover, the methoxy-group in the azepines is replaceable by amines.

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