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CAS

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1196508-40-3

4-methyldeca-4,5-dienyl benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1196508-40-3 Structure

  • Basic information

    1. Product Name: 4-methyldeca-4,5-dienyl benzoate
    2. Synonyms: 4-methyldeca-4,5-dienyl benzoate
    3. CAS NO:1196508-40-3
    4. Molecular Formula:
    5. Molecular Weight: 272.387
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1196508-40-3.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: 4-methyldeca-4,5-dienyl benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-methyldeca-4,5-dienyl benzoate(1196508-40-3)
    11. EPA Substance Registry System: 4-methyldeca-4,5-dienyl benzoate(1196508-40-3)

  • 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: 1196508-40-3(Hazardous Substances Data)

1196508-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1196508-40-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,6,5,0 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1196508-40:
(9*1)+(8*1)+(7*9)+(6*6)+(5*5)+(4*0)+(3*8)+(2*4)+(1*0)=173
173 % 10 = 3
So 1196508-40-3 is a valid CAS Registry Number.

1196508-40-3Downstream Products

1196508-40-3Relevant articles and documents

The synthesis of allenes by Cu(i)-catalyzed regio- and stereoselective reduction of propargylic carbonates with hydrosilanes

Zhong, Chongmin,Sasaki, Yusuke,Ito, Hajime,Sawamura, Masaya

, p. 5850 - 5852 (2009)

Cu(i)-catalyzed anti-SN2′-type reduction of internal propargylic carbonates with hydrosilanes affords various di- and trisubstituted allenes with high regioselectivities; the reactions are compatible with functional groups and work efficiently

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