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2-oxo-9-phenyl-3H,10H-furo<3,4-f>benzo<1.4>diazepine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138196-67-5

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  • 138196-67-5 Structure

  • Basic information

    1. Product Name: 2-oxo-9-phenyl-3H,10H-furo<3,4-f>benzo<1.4>diazepine
    2. Synonyms:
    3. CAS NO:138196-67-5
    4. Molecular Formula:
    5. Molecular Weight: 276.294
    6. EINECS: N/A
    7. Product Categories: N/A

  • 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: 2-oxo-9-phenyl-3H,10H-furo<3,4-f>benzo<1.4>diazepine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-oxo-9-phenyl-3H,10H-furo<3,4-f>benzo<1.4>diazepine(138196-67-5)
    11. EPA Substance Registry System: 2-oxo-9-phenyl-3H,10H-furo<3,4-f>benzo<1.4>diazepine(138196-67-5)

  • 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: 138196-67-5(Hazardous Substances Data)

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138196-67-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138196-67-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,1,9 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 138196-67:
(8*1)+(7*3)+(6*8)+(5*1)+(4*9)+(3*6)+(2*6)+(1*7)=155
155 % 10 = 5
So 138196-67-5 is a valid CAS Registry Number.

138196-67-5Downstream Products

138196-67-5Relevant academic research and scientific papers

Substituted γ-Lactones: On the Structural Elucidation of the Reaction Products from 4-Aroyl-3-hydroxy-2(5H)-furanones and 1,2-Diamines

Zimmer, Hans,Amer, Adel,Ho, Douglas,Palmer-Sungail, R.

, p. 1501 - 1510 (2007/10/02)

The reaction pathway of 4-aroyl-3-hydroxy-2(5H)-furanones 1 with diamines depends on the nature of the amine as well as on the applied reaction conditions.Thus, the reaction of 1a-d with 5,6-diamino-1,3-dimethyluracil 5 led to the formation of two isomeri

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