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benzocyclohept<1,4>oxazin-6(11H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70664-12-9

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  • 70664-12-9 Structure
  • Basic information

    1. Product Name: benzocyclohept<1,4>oxazin-6(11H)-one
    2. Synonyms:
    3. CAS NO:70664-12-9
    4. Molecular Formula:
    5. Molecular Weight: 211.22
    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: benzocyclohept<1,4>oxazin-6(11H)-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzocyclohept<1,4>oxazin-6(11H)-one(70664-12-9)
    11. EPA Substance Registry System: benzocyclohept<1,4>oxazin-6(11H)-one(70664-12-9)
  • 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: 70664-12-9(Hazardous Substances Data)

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70664-12-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70664-12-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,6 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 70664-12:
(7*7)+(6*0)+(5*6)+(4*6)+(3*4)+(2*1)+(1*2)=119
119 % 10 = 9
So 70664-12-9 is a valid CAS Registry Number.

70664-12-9Downstream Products

70664-12-9Relevant 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.

Reactive Troponoids and o-Aminophenol. V. The Reaction of 3-Bromo-2-methoxytropone and o-Aminophenol

Someya, Taichi,Okai, Harue,Wakabayashi, Hidetsugu,Nozoe, Tetsuo

, p. 2756 - 2761 (2007/10/02)

The reaction products of the title substances in hot acetic acid were separated by preparative TLC into compounds A-L according to the Rf-values, and the structural assignments for these products were now made as follows: A, 14H-benzoxazinocycloheptabenzoxazine; B, 1-formylphenoxazine; F, cycloheptadibenzoxazine; G, cycloheptabenzoxazin-10(11H)-one or its enolic form; J, cycloheptabenzoxazin-6(11H)-one; L, 6-(o-hydroxyanilino)cycloheptabenzoxazine hydrobromide. A small amount of 2-methylamino-3H-phenoxazin-3-one was also produced. Possible reaction pathways for the formation of these products are also discussed.

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