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3-nitro-12H-benzophenoxazine-6,11-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75197-88-5

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  • 75197-88-5 Structure
  • Basic information

    1. Product Name: 3-nitro-12H-benzophenoxazine-6,11-dione
    2. Synonyms:
    3. CAS NO:75197-88-5
    4. Molecular Formula:
    5. Molecular Weight: 308.25
    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: 3-nitro-12H-benzophenoxazine-6,11-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-nitro-12H-benzophenoxazine-6,11-dione(75197-88-5)
    11. EPA Substance Registry System: 3-nitro-12H-benzophenoxazine-6,11-dione(75197-88-5)
  • 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: 75197-88-5(Hazardous Substances Data)

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75197-88-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75197-88-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,9 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 75197-88:
(7*7)+(6*5)+(5*1)+(4*9)+(3*7)+(2*8)+(1*8)=165
165 % 10 = 5
So 75197-88-5 is a valid CAS Registry Number.

75197-88-5Downstream Products

75197-88-5Relevant academic research and scientific papers

Quinone Chemistry. Reaction of 2,3-Dichloro-1,4-naphthoquinone with 2-Aminophenols in Pyridine

Agarwal, Nand L.,Schaefer, Wolfram

, p. 5144 - 5149 (2007/10/02)

The reaction of 2,3-dichloro-1,4-naphthoquinone (1) and 2-aminophenols (2) in pyridine furnished substituted 6-chloro-5H-benzophenoxazin-5-one (10), 5H-benzophenoxazin-5-one (8), 5H-benzophenoxazin-5-one-6-pyridinium chloride (6), 2-(2-hydroxyanilino)-1,4-naphthoquinone-3-pyridinium chloride (5), and 12H-benzophenoxazine-6,11-dione (7).It was observed that the nature and yields of the reaction products were greatly influenced by the substituent present in 2.The reaction mechanism for the formation of all products is discussed, and spectroscopic data are also given.This reaction for the first time led to a development of a novel, convenient synthesis of a new class of heterocyclic quinones (7).

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