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[4-(bromo-difluoro-methoxy)-phenyl]-(4-chloro-phenyl)-methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 229027-51-4 Structure
  • Basic information

    1. Product Name: [4-(bromo-difluoro-methoxy)-phenyl]-(4-chloro-phenyl)-methanone
    2. Synonyms: [4-(bromo-difluoro-methoxy)-phenyl]-(4-chloro-phenyl)-methanone
    3. CAS NO:229027-51-4
    4. Molecular Formula:
    5. Molecular Weight: 361.57
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 229027-51-4.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: [4-(bromo-difluoro-methoxy)-phenyl]-(4-chloro-phenyl)-methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: [4-(bromo-difluoro-methoxy)-phenyl]-(4-chloro-phenyl)-methanone(229027-51-4)
    11. EPA Substance Registry System: [4-(bromo-difluoro-methoxy)-phenyl]-(4-chloro-phenyl)-methanone(229027-51-4)
  • 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: 229027-51-4(Hazardous Substances Data)

229027-51-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 229027-51-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,9,0,2 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 229027-51:
(8*2)+(7*2)+(6*9)+(5*0)+(4*2)+(3*7)+(2*5)+(1*1)=124
124 % 10 = 4
So 229027-51-4 is a valid CAS Registry Number.

229027-51-4Relevant articles and documents

Synthesis and structure-activity relationships of benzophenone hydrazone derivatives with insecticidal activity

Boeger, Manfred,Duerr, Dieter,Gsell, Laurenz,Hall, Roger G.,Karrer, Friedrich,Kristiansen, Odd,Maienfisch, Peter,Pascual, Alfons,Rindlisbacher, Alfred

, p. 191 - 202 (2007/10/03)

A broad range of benzophenone hydrazone derivatives was prepared and tested against selected chewing insect pests, allowing the analysis of structure-activity relationships. Good activity was found only when the aromatic rings were substituted at the 4-positions with an halogen atom and a triflate or perhaloalkoxy group. In contrast, a number of substituents on the hydrazone part led to active compounds, the best results being achieved with acyl-type substituents. The excellent laboratory and greenhouse activity of the best representatives was confirmed in semi-field trials against Spodoptera littoralis. ° 2001 Society of Chemical Industry.

Synthesis and insecticidal activity of 4-perhaloalkoxy (or thioalkyl) benzophenonehydrazone derivatives

Duerr, Dieter,Gsell, Laurenz,Hall, Roger G.,Karrer, Friedrich,Pascual, Alfons,Rindlisbacher, Alfred

, p. 584 - 587 (2007/10/03)

Benzophenonehydrazone derivatives containing a mesylate or triflate substituent are known to exhibit insecticidal activity. In the present study, such substituents have been replaced by perhaloalkoxy groups. High levels of activity against lepidopteran pests were observed in greenhouse trials. For optimum activity, the substituents should be relatively small. In semi-field trials, however, none of the compounds tested showed sufficient persistence to warrant further development.

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