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diphenylmethyl (2-((diphenylmethoxy)carbonyl)benzofuran-3-yl)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

131353-38-3

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  • 131353-38-3 Structure

  • Basic information

    1. Product Name: diphenylmethyl (2-((diphenylmethoxy)carbonyl)benzofuran-3-yl)acetate
    2. Synonyms:
    3. CAS NO:131353-38-3
    4. Molecular Formula:
    5. Molecular Weight: 552.626
    6. EINECS: N/A
    7. Product Categories: N/A

  • 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: diphenylmethyl (2-((diphenylmethoxy)carbonyl)benzofuran-3-yl)acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: diphenylmethyl (2-((diphenylmethoxy)carbonyl)benzofuran-3-yl)acetate(131353-38-3)
    11. EPA Substance Registry System: diphenylmethyl (2-((diphenylmethoxy)carbonyl)benzofuran-3-yl)acetate(131353-38-3)

  • 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: 131353-38-3(Hazardous Substances Data)

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131353-38-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131353-38-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,3,5 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 131353-38:
(8*1)+(7*3)+(6*1)+(5*3)+(4*5)+(3*3)+(2*3)+(1*8)=93
93 % 10 = 3
So 131353-38-3 is a valid CAS Registry Number.

131353-38-3Relevant academic research and scientific papers

Strong-Base-Induced Intramolecular Cycloaddition of Homophthalic Anhydrides: An Efficient Synthesis of Polycyclic peri-Hydroxy Aromatic Compounds

Kita, Yasuyuki,Okunaka, Ryuichi,Honda, Takao,Shindo, Miki,Taniguchi, Miyako,et al.

, p. 119 - 125 (2007/10/02)

A strong-base-induced intramolecular cycloaddition reaction of homophthalic anhydrides has been examined as a method for preparing nonlinear polycyclic peri-hydroxy aromatic compounds.

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