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2-(2-furoyl)benzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 69763-71-9 Structure
  • Basic information

    1. Product Name: 2-(2-furoyl)benzaldehyde
    2. Synonyms: 2-(2-furoyl)benzaldehyde
    3. CAS NO:69763-71-9
    4. Molecular Formula: C12H8O3
    5. Molecular Weight: 200.19012
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 69763-71-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(2-furoyl)benzaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2-furoyl)benzaldehyde(69763-71-9)
    11. EPA Substance Registry System: 2-(2-furoyl)benzaldehyde(69763-71-9)
  • 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: 69763-71-9(Hazardous Substances Data)

69763-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69763-71-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,6 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69763-71:
(7*6)+(6*9)+(5*7)+(4*6)+(3*3)+(2*7)+(1*1)=179
179 % 10 = 9
So 69763-71-9 is a valid CAS Registry Number.

69763-71-9Downstream Products

69763-71-9Relevant articles and documents

Facile Sc(OTf)3-catalyzed generation and successive aromatization of isobenzofuran from o -dicarbonylbenzenes

Nishina, Yuta,Kida, Tatsuya,Ureshino, Tomonari

, p. 3960 - 3963 (2011/10/01)

Isobenzofuran can be prepared from o-phthalaldehyde using hydrosilane. The formed isobenzofuran is trapped by an alkene via a Diels-Alder reaction. Further dehydration proceeds to furnish the conjugated aromatic compound. This multistep reaction was promoted by catalytic amounts of Sc(OTf)3.

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