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CAS

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1129399-42-3

1-(allyloxy)-6-(4-(trifluoromethyl)phenyl)-3a,4-dihydro-1H-cyclopenta[c]furan-5(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1129399-42-3 Structure

  • Basic information

    1. Product Name: 1-(allyloxy)-6-(4-(trifluoromethyl)phenyl)-3a,4-dihydro-1H-cyclopenta[c]furan-5(3H)-one
    2. Synonyms:
    3. CAS NO:1129399-42-3
    4. Molecular Formula:
    5. Molecular Weight: 324.3
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1129399-42-3.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: 1-(allyloxy)-6-(4-(trifluoromethyl)phenyl)-3a,4-dihydro-1H-cyclopenta[c]furan-5(3H)-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(allyloxy)-6-(4-(trifluoromethyl)phenyl)-3a,4-dihydro-1H-cyclopenta[c]furan-5(3H)-one(1129399-42-3)
    11. EPA Substance Registry System: 1-(allyloxy)-6-(4-(trifluoromethyl)phenyl)-3a,4-dihydro-1H-cyclopenta[c]furan-5(3H)-one(1129399-42-3)

  • 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: 1129399-42-3(Hazardous Substances Data)

1129399-42-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1129399-42-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,9,3,9 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1129399-42:
(9*1)+(8*1)+(7*2)+(6*9)+(5*3)+(4*9)+(3*9)+(2*4)+(1*2)=173
173 % 10 = 3
So 1129399-42-3 is a valid CAS Registry Number.

1129399-42-3Downstream Products

1129399-42-3Relevant articles and documents

Asymmetric desymmetrization of the diallyl acetals of alkynals by the enantioselective Pauson-Khand-type reaction catalysts

Dong, Eun Kim,Bo, Hyung Lee,Rajagopalasarma, Mudigonda,Genet, Jean-Pierre,Ratovelomanana-Vidal, Virginie,Jeong, Nakcheol

, p. 2695 - 2700 (2008)

Asymmetric desymmetrization of the di-allyl acetals of alkynal (1) by an enantioselective Pauson-Khand-type reaction catalyst was studied. The corresponding 5-oxabicyclo[3.3.0]octenones (2) were obtained as a mixture of diastereomers (2a and 2b), which were hydrolyzed to afford a single enantiomer (3), in high yields (up to 88%) as well as excellent enantioselectivities (up to 97%).

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