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10-(o-hydroxyanilino)cyclohepta<1,4>benzoxazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

120624-23-9

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  • 120624-23-9 Structure

  • Basic information

    1. Product Name: 10-(o-hydroxyanilino)cyclohepta<1,4>benzoxazine
    2. Synonyms:
    3. CAS NO:120624-23-9
    4. Molecular Formula:
    5. Molecular Weight: 302.332
    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: 10-(o-hydroxyanilino)cyclohepta<1,4>benzoxazine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 10-(o-hydroxyanilino)cyclohepta<1,4>benzoxazine(120624-23-9)
    11. EPA Substance Registry System: 10-(o-hydroxyanilino)cyclohepta<1,4>benzoxazine(120624-23-9)

  • 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: 120624-23-9(Hazardous Substances Data)

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120624-23-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120624-23-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,6,2 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 120624-23:
(8*1)+(7*2)+(6*0)+(5*6)+(4*2)+(3*4)+(2*2)+(1*3)=79
79 % 10 = 9
So 120624-23-9 is a valid CAS Registry Number.

120624-23-9Downstream Products

120624-23-9Relevant academic research and scientific papers

Cycloheptabenzoxazines 3. The Reaction of 6-Bromocycloheptabenzoxazine with o-Aminophenol

Nozoe, Tetsuo,Okai, Harue,Wakabayashi, Hidetsugu,Ishikawa, Sumio

, p. 2307 - 2314 (2007/10/02)

The reaction of 6-bromocycloheptabenzoxazine (19) and o-aminophenol (3) was studied and compared with that of 3-bromo-2-methoxytropone (2) with 3. 14H-Benzoxazinocycloheptabenzoxazine, 10-(o-hydroxyanilino)cycloheptabenzoxazine (D), 1- and 4-formylphenoxazines and their Schiff bases (C and X) were obtained in very good yields by modifying the conditions of the reaction of 19 with 3.Structures of D, C, and their isomers were determined and the possible reaction pathways for the formation of various products are discussed.

Novel Intermolecular Heterocycle Exchange Reaction of Cycloheptabenzoxazines with o-Aminophenol Derivatives

Nozoe, Tetsuo,Okai, Harue,Wakabayashi, Hidetsugu,Ishikawa, Sumio

, p. 1589 - 1592 (2007/10/02)

The benzoxazine moiety of 7-, 8-, and 9-isopropyl- as well as 6-bromocycloheptabenzoxazines was easily exchanged with o-aminophenol and its methyl derivatives in methanol or acetic acid.A possible pathway of this novel intermolecular heterocycle exchange reaction is discussed.

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