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C15H13BrO2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1441127-82-7 Structure
  • Basic information

    1. Product Name: C15H13BrO2
    2. Synonyms: C15H13BrO2
    3. CAS NO:1441127-82-7
    4. Molecular Formula:
    5. Molecular Weight: 305.171
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1441127-82-7.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: C15H13BrO2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C15H13BrO2(1441127-82-7)
    11. EPA Substance Registry System: C15H13BrO2(1441127-82-7)
  • 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: 1441127-82-7(Hazardous Substances Data)

1441127-82-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1441127-82-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,1,1,2 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1441127-82:
(9*1)+(8*4)+(7*4)+(6*1)+(5*1)+(4*2)+(3*7)+(2*8)+(1*2)=127
127 % 10 = 7
So 1441127-82-7 is a valid CAS Registry Number.

1441127-82-7Downstream Products

1441127-82-7Relevant articles and documents

The Michael addition of 1,2-cyclohexanedione to β-nitrostyrenes (I): The synthesis of 3-aryl-5,6-dihydrobenzofuran-7(4H)-ones

Simpkins, Chad M.,Hunt, David A.

, p. 3371 - 3373 (2013)

The reaction of β-nitrostyrenes with 1,2-cyclohexanedione using K 2CO3 as a base results in the formation of 3-aryl-5,6-dihydrobenzofuran-7(4H)-ones in good yields. A putative reaction mechanism involves an initial Michael addition of the dione C-enolate to the β-nitro-styrene, followed by intramolecular cyclization of the resulting O-enolate anion, elimination of nitrite ion, and air oxidation. Product formation is highly dependent on base stoichiometry.

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