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132541-04-9

cis-1-acetoxy-4-(dicarbomethoxymethyl)-2-cyclohexene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132541-04-9 Structure

  • Basic information

    1. Product Name: cis-1-acetoxy-4-(dicarbomethoxymethyl)-2-cyclohexene
    2. Synonyms:
    3. CAS NO:132541-04-9
    4. Molecular Formula:
    5. Molecular Weight: 270.282
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132541-04-9.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: cis-1-acetoxy-4-(dicarbomethoxymethyl)-2-cyclohexene(CAS DataBase Reference)
    10. NIST Chemistry Reference: cis-1-acetoxy-4-(dicarbomethoxymethyl)-2-cyclohexene(132541-04-9)
    11. EPA Substance Registry System: cis-1-acetoxy-4-(dicarbomethoxymethyl)-2-cyclohexene(132541-04-9)

  • 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: 132541-04-9(Hazardous Substances Data)

132541-04-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132541-04-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,5,4 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132541-04:
(8*1)+(7*3)+(6*2)+(5*5)+(4*4)+(3*1)+(2*0)+(1*4)=89
89 % 10 = 9
So 132541-04-9 is a valid CAS Registry Number.

132541-04-9Relevant articles and documents

Palladium-catalyzed substitution of allylic fluorides

Hazari, Amaruka,Gouverneur, Ve,Brown, John M.

, p. 1296 - 1299 (2009)

As unusual substrates for the Tsuji-Trost allylation reaction, allylic fluorides are responsive to palladiumcatalyzed substitution. Their activity towards this reaction fits in the series OCO2Me>OBz? F? OAc. The classic stereoretention mechanis

Stereoselective Synthesis of Vinylcyclopropanes via Palladium-Catalyzed Reactions

Baeckvall, J. E.,Vagberg, J. O.,Zercher, C.,Genet, J. P.,Denis, A.

, p. 5430 - 5435 (2007/10/02)

Vinylcyclopropanes were synthesized in a stereocontrolled manner from 1-acetoxy-4-chloro-2-alkenes.A stereospecific palladium-catalyzed substitution of the chloro group by dimethyl malonate anion and subsequent palladium-catalyzed cyclization afforded the

STEREOSPECIFIC PALLADIUM-CATALYZED 1,4-ACETOXYCHLORINATION OF 1,3-DIENES

Baeckvall, Jan-E.,Nordberg, Ruth E.,Nystroem, Jan-E.

, p. 1617 - 1620 (2007/10/02)

Palladium-catalyzed oxidation of 1,3-dienes in acetic acid in the presence of LiCl and LiOAc produces 1-acetoxy-4-chloro-2-alkenes in high selectivity.The 1,4-adducts were stereo- and regioselectively functionalized.

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