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CAS

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1043044-05-8

C32H32O8 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1043044-05-8 Structure

  • Basic information

    1. Product Name: C32H32O8
    2. Synonyms: C32H32O8
    3. CAS NO:1043044-05-8
    4. Molecular Formula:
    5. Molecular Weight: 544.601
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1043044-05-8.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: C32H32O8(CAS DataBase Reference)
    10. NIST Chemistry Reference: C32H32O8(1043044-05-8)
    11. EPA Substance Registry System: C32H32O8(1043044-05-8)

  • 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: 1043044-05-8(Hazardous Substances Data)

1043044-05-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1043044-05-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,3,0,4 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1043044-05:
(9*1)+(8*0)+(7*4)+(6*3)+(5*0)+(4*4)+(3*4)+(2*0)+(1*5)=88
88 % 10 = 8
So 1043044-05-8 is a valid CAS Registry Number.

1043044-05-8Downstream Products

1043044-05-8Relevant articles and documents

Pd-catalyzed borylative polycyclization of enediynes to allylboronates

Marco-Martinez, Juan,Bunuel, Elena,Munoz-Rodriguez, Rebeca,Cardenas, Diego J.

, p. 3619 - 3621 (2008)

(Chemical Equation Presented) Pd-catalyzed dicyclization of 6-ene-1,11-diynes with bis(pinacolato)diboron affords synthetically useful allylboronates under smooth conditions. Two new C-C and one C-B bonds are stereospecifically formed in a single operation. The stereochemical outcome depends on the starting alkene configuration. The reaction is general and has been applied to differently substituted enediynes. Isolation of intermediate 1,3-dienes suggests a regioselective β-hydrogen elimination along the reaction pathway.

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