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107821-10-3

3,3-dimethyl-5-phenyl-valeric acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 107821-10-3 Structure

  • Basic information

    1. Product Name: 3,3-dimethyl-5-phenyl-valeric acid methyl ester
    2. Synonyms: 3,3-dimethyl-5-phenyl-valeric acid methyl ester
    3. CAS NO:107821-10-3
    4. Molecular Formula:
    5. Molecular Weight: 220.312
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 107821-10-3.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: 3,3-dimethyl-5-phenyl-valeric acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,3-dimethyl-5-phenyl-valeric acid methyl ester(107821-10-3)
    11. EPA Substance Registry System: 3,3-dimethyl-5-phenyl-valeric acid methyl ester(107821-10-3)

  • 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: 107821-10-3(Hazardous Substances Data)

107821-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107821-10-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,8,2 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 107821-10:
(8*1)+(7*0)+(6*7)+(5*8)+(4*2)+(3*1)+(2*1)+(1*0)=103
103 % 10 = 3
So 107821-10-3 is a valid CAS Registry Number.

107821-10-3Relevant articles and documents

Ligand-Enabled γ-C(sp3)?H Olefination of Free Carboxylic Acids

Ghiringhelli, Francesca,Ghosh, Kiron Kumar,Mondal, Arup,Uttry, Alexander,Wedi, Philipp,van Gemmeren, Manuel

, p. 12848 - 12852 (2020)

We report the ligand-enabled C?H activation/olefination of free carboxylic acids in the γ-position. Through an intramolecular Michael addition, δ-lactones are obtained as products. Two distinct ligand classes are identified that enable the challenging palladium-catalyzed activation of free carboxylic acids in the γ-position. The developed protocol features a wide range of acid substrates and olefin reaction partners and is shown to be applicable on a preparatively useful scale. Insights into the underlying reaction mechanism obtained through kinetic studies are reported.

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