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1023961-35-4

3-(2-bromophenyl)-2,6-dimethyl-4H-pyran-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1023961-35-4 Structure

  • Basic information

    1. Product Name: 3-(2-bromophenyl)-2,6-dimethyl-4H-pyran-4-one
    2. Synonyms: 3-(2-bromophenyl)-2,6-dimethyl-4H-pyran-4-one
    3. CAS NO:1023961-35-4
    4. Molecular Formula:
    5. Molecular Weight: 279.133
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1023961-35-4.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: 3-(2-bromophenyl)-2,6-dimethyl-4H-pyran-4-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(2-bromophenyl)-2,6-dimethyl-4H-pyran-4-one(1023961-35-4)
    11. EPA Substance Registry System: 3-(2-bromophenyl)-2,6-dimethyl-4H-pyran-4-one(1023961-35-4)

  • 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: 1023961-35-4(Hazardous Substances Data)

1023961-35-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1023961-35-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,3,9,6 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1023961-35:
(9*1)+(8*0)+(7*2)+(6*3)+(5*9)+(4*6)+(3*1)+(2*3)+(1*5)=124
124 % 10 = 4
So 1023961-35-4 is a valid CAS Registry Number.

1023961-35-4Relevant articles and documents

Synthesis and structure-activity relationships of 4-pyridones as potential antimalarials

Yeates, Clive L.,Batchelor, John F.,Capon, Edward C.,Cheesman, Neil J.,Fry, Mitch,Hudson, Alan T.,Pudney, Mary,Trimming, Helen,Woolven, James,Bueno, José M.,Chicharro, Jesús,Fernández, Esther,Fiandor, José M.,Gargallo-Viola, Domingo,De Las Heras, Federico Gómez,Herreros, Esperanza,León, María L.

, p. 2845 - 2852 (2008/12/23)

A series of diaryl ether substituted 4-pyridones have been identified as having potent antimalarial activity superior to that of chloroquine against Plasmodium falciparum in vitro and murine Plasmodium yoelii in vivo. These were derived from the anticoccidial drug clopidol through a systematic study of the effects of varying the side chain on activity. Relative to clopidol the most active compounds show > 500-fold improvement in IC50 for inhibition of P. falciparum in vitro and about 100-fold improvement with respect to ED50 against P. yoelii in mice. These compounds have been shown elsewhere to act selectively by inhibition of mitochondrial electron transport at the cytochrome bc1 complex.

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