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101404-06-2

o-methyleneacetoxy-phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 101404-06-2 Structure

  • Basic information

    1. Product Name: o-methyleneacetoxy-phenol
    2. Synonyms: o-methyleneacetoxy-phenol
    3. CAS NO:101404-06-2
    4. Molecular Formula:
    5. Molecular Weight: 164.161
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 101404-06-2.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: o-methyleneacetoxy-phenol(CAS DataBase Reference)
    10. NIST Chemistry Reference: o-methyleneacetoxy-phenol(101404-06-2)
    11. EPA Substance Registry System: o-methyleneacetoxy-phenol(101404-06-2)

  • 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: 101404-06-2(Hazardous Substances Data)

101404-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101404-06-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,4,0 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 101404-06:
(8*1)+(7*0)+(6*1)+(5*4)+(4*0)+(3*4)+(2*0)+(1*6)=52
52 % 10 = 2
So 101404-06-2 is a valid CAS Registry Number.

101404-06-2Downstream Products

101404-06-2Relevant articles and documents

Enantioselective synthesis of amaryllidaceae alkaloids (+)-vittatine, (+)-epi-vittatine, and (+)-buphanisine

Wei, Meng-Xue,Wang, Cheng-Tao,Du, Ji-Yuan,Qu, Hu,Yin, Pei-Rong,Bao, Xu,Ma, Xiao-Yan,Zhao, Xian-He,Zhang, Guo-Biao,Fan, Chun-An

, p. 1966 - 1971 (2013)

Cat. on a hot tin roof: Enantioselective catalytic Michael addition of α-cyanoketones to acrylates under bifunctional organocatalysis was used to construct the unique arylic all-carbon quaternary stereocenter, which is synthetically crucial in the chemical synthesis of optically pure cis-aryl hydroindole alkaloids. The protocol offers an asymmetric route to (+)-vittatine, (+)-epi-vittatine, and (+)-buphanisine. Copyright

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