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107625-40-1

3-methyl-6-oxo-6-phenyl-hex-2ξ-enoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 107625-40-1 Structure

  • Basic information

    1. Product Name: 3-methyl-6-oxo-6-phenyl-hex-2ξ-enoic acid
    2. Synonyms: 3-methyl-6-oxo-6-phenyl-hex-2ξ-enoic acid
    3. CAS NO:107625-40-1
    4. Molecular Formula:
    5. Molecular Weight: 218.252
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 107625-40-1.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-methyl-6-oxo-6-phenyl-hex-2ξ-enoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-methyl-6-oxo-6-phenyl-hex-2ξ-enoic acid(107625-40-1)
    11. EPA Substance Registry System: 3-methyl-6-oxo-6-phenyl-hex-2ξ-enoic acid(107625-40-1)

  • 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: 107625-40-1(Hazardous Substances Data)

107625-40-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107625-40-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,6,2 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 107625-40:
(8*1)+(7*0)+(6*7)+(5*6)+(4*2)+(3*5)+(2*4)+(1*0)=111
111 % 10 = 1
So 107625-40-1 is a valid CAS Registry Number.

107625-40-1Downstream Products

107625-40-1Relevant articles and documents

Rh/Cu-Catalyzed Ketone β-Functionalization by Merging Ketone Dehydrogenation and Carboxyl-Directed C-H Alkylation

Li, Hongyi,Jiang, Quandi,Jie, Xiaoming,Shang, Yaping,Zhang, Yuanfei,Goossen, Lukas J.,Su, Weiping

, p. 4777 - 4782 (2018)

An efficient Rh/Cu-catalyzed method has been developed for the direct β-arylation or alkenylation of ketones using (hetero)aryl or alkenyl carboxylic acids as coupling partners. This direct ketone β-functionalization reaction proceeded via the merging of Cu-catalyzed ketone dehydrogenative desaturation and Rh-catalyzed carboxyl-directed C-H alkylation, exhibiting a broad substrate scope for both coupling partners. TEMPO proved to be essential for both dehydrogenation process and generation of the active Rh catalyst for C-H activation.

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