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  • 1431629-79-6 Structure
  • Basic information

    1. Product Name: C28H22O2
    2. Synonyms:
    3. CAS NO:1431629-79-6
    4. Molecular Formula:
    5. Molecular Weight: 390.481
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1431629-79-6.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: C28H22O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C28H22O2(1431629-79-6)
    11. EPA Substance Registry System: C28H22O2(1431629-79-6)
  • 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: 1431629-79-6(Hazardous Substances Data)

1431629-79-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1431629-79-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,1,6,2 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1431629-79:
(9*1)+(8*4)+(7*3)+(6*1)+(5*6)+(4*2)+(3*9)+(2*7)+(1*9)=156
156 % 10 = 6
So 1431629-79-6 is a valid CAS Registry Number.

1431629-79-6Upstream product

1431629-79-6Downstream Products

1431629-79-6Relevant articles and documents

Resveratrol-related dehydrodimers: Laccase-mediated biomimetic synthesis and antiproliferative activity

Bhusainahalli, Vedamurthy M.,Spatafora, Carmela,Chalal, Malik,Vervandier-Fasseur, Dominique,Meunier, Philippe,Latruffe, Norbert,Tringali, Corrado

, p. 5217 - 5224 (2012)

Seven resveratrol-related monomeric stilbenoids were submitted to biomimetic oxidative coupling in the presence of laccase from Trametes versicolor (TvL), and gave racemic dihydrobenzofuran dehydrodimers (±)-15 to (±)-21. These products, after spectral characterization, were submitted to an antiproliferative activity bioassay against SW480 human colon cancer cells. Five racemates were found to be active, and were resolved by chiral HPLC. The pure enantiomers were subjected to circular dichroism measurements to establish their absolute configurations at C-7 and C-8. These enantiomerically pure compounds were submitted to the antiproliferative activity assay towards SW480 cells, and were all shown to be active with IC50 values in the approximate range 20-90 μM. In some cases, a significant difference between the activity of the 7R,8R and 7S,8S enantiomers was observed, but a defined configuration of the stereogenic centers does not appear to be a structural requirement for the activity. The comparison between the most active compounds and the inactive ones strongly suggests that the presence of a methoxy group in the position ortho to the C-4 hydroxy group is highly detrimental to the activity. Copyright

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