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CAS

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625825-20-9

6-chloro-4-methylidene-3-[N-phenylamino]-3,4-dihydro-2H-1,3-benzoxazin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 625825-20-9 Structure

  • Basic information

    1. Product Name: 6-chloro-4-methylidene-3-[N-phenylamino]-3,4-dihydro-2H-1,3-benzoxazin-2-one
    2. Synonyms:
    3. CAS NO:625825-20-9
    4. Molecular Formula:
    5. Molecular Weight: 286.718
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 625825-20-9.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: 6-chloro-4-methylidene-3-[N-phenylamino]-3,4-dihydro-2H-1,3-benzoxazin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-chloro-4-methylidene-3-[N-phenylamino]-3,4-dihydro-2H-1,3-benzoxazin-2-one(625825-20-9)
    11. EPA Substance Registry System: 6-chloro-4-methylidene-3-[N-phenylamino]-3,4-dihydro-2H-1,3-benzoxazin-2-one(625825-20-9)

  • 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: 625825-20-9(Hazardous Substances Data)

625825-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 625825-20-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,5,8,2 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 625825-20:
(8*6)+(7*2)+(6*5)+(5*8)+(4*2)+(3*5)+(2*2)+(1*0)=159
159 % 10 = 9
So 625825-20-9 is a valid CAS Registry Number.

625825-20-9Downstream Products

625825-20-9Relevant articles and documents

Synthesis of 4-alkoxy-4-methyl- and 4-alkoxy-4-fluoromethyl-1,3-benzoxazinones

Alkhathlan, Hamad Z.

, p. 8163 - 8170 (2003)

Cyclization of 2-hydroxyacetophenone hydrazones with triphosgene resulted in the formation of 4-methylene-1,3-benzoxazinones. These compounds were converted to 4-alkoxy-4-methyl-1,3-benzoxazinones and 4-fluoromethyl-4-methoxy-1,3-benzoxazinones upon treatment with alcohols under refluxing conditions and F-TEDA-BF4 in acetonitrile and methanol, respectively.

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