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928712-61-2

α-Hydroxy-4-methoxy-α-phenylbenzeneacetic 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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  • 928712-61-2 Structure

  • Basic information

    1. Product Name: α-Hydroxy-4-methoxy-α-phenylbenzeneacetic acid methyl ester
    2. Synonyms: α-Hydroxy-4-methoxy-α-phenylbenzeneacetic acid methyl ester
    3. CAS NO:928712-61-2
    4. Molecular Formula:
    5. Molecular Weight: 272.301
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 928712-61-2.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: α-Hydroxy-4-methoxy-α-phenylbenzeneacetic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: α-Hydroxy-4-methoxy-α-phenylbenzeneacetic acid methyl ester(928712-61-2)
    11. EPA Substance Registry System: α-Hydroxy-4-methoxy-α-phenylbenzeneacetic acid methyl ester(928712-61-2)

  • 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: 928712-61-2(Hazardous Substances Data)

928712-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 928712-61-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,8,7,1 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 928712-61:
(8*9)+(7*2)+(6*8)+(5*7)+(4*1)+(3*2)+(2*6)+(1*1)=192
192 % 10 = 2
So 928712-61-2 is a valid CAS Registry Number.

928712-61-2Relevant articles and documents

Synthesis of Chiral Triarylmethanes Bearing All-Carbon Quaternary Stereocenters: Catalytic Asymmetric Oxidative Cross-Coupling of 2,2-Diarylacetonitriles and (Hetero)arenes

Wang, Zehua,Zhu, Yasheng,Pan, Xiaoguang,Wang, Gang,Liu, Lei

, p. 3053 - 3057 (2020)

A direct and enantioselective oxidative cross-coupling of racemic 2,2-diarylacetonitriles with electron-rich (hetero)arenes has been described, which allows for efficient construction of triarylmethanes bearing all-carbon quaternary stereocenters with excellent chemo- and enantioselectivity. The reaction has an excellent functional group tolerance, and exhibits a broad scope with respect to both 2,2-diarylacetonitrile and (hetero)arene components. The rich chemistry of the cyano group allows for facile synthesis of other valuable chiral triarylmethanes bearing all-carbon quaternary centers that are otherwise difficult to access.

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