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2-acetyl-4-benzyloxy-4,5,6,7-tetrahydrobenzofuran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

120085-90-7

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  • 120085-90-7 Structure

  • Basic information

    1. Product Name: 2-acetyl-4-benzyloxy-4,5,6,7-tetrahydrobenzofuran
    2. Synonyms:
    3. CAS NO:120085-90-7
    4. Molecular Formula:
    5. Molecular Weight: 270.328
    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: 2-acetyl-4-benzyloxy-4,5,6,7-tetrahydrobenzofuran(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-acetyl-4-benzyloxy-4,5,6,7-tetrahydrobenzofuran(120085-90-7)
    11. EPA Substance Registry System: 2-acetyl-4-benzyloxy-4,5,6,7-tetrahydrobenzofuran(120085-90-7)

  • 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: 120085-90-7(Hazardous Substances Data)

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120085-90-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120085-90-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,0,8 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 120085-90:
(8*1)+(7*2)+(6*0)+(5*0)+(4*8)+(3*5)+(2*9)+(1*0)=87
87 % 10 = 7
So 120085-90-7 is a valid CAS Registry Number.

120085-90-7Downstream Products

120085-90-7Relevant academic research and scientific papers

Intramolecular Cycloadditions of Mesionic Carbonyl Ylides with Alkynes. Synthesis of 5,6-Dihydro-4H-cyclopenta- and 4,5,6,7-Tetrahydrobenzofuran Derivatives

Maier, Martin E.,Schoeffling, Baerbel

, p. 1081 - 1088 (2007/10/02)

Intramolecular cycloaddition reactions of acetylenic isomuenchnones, formed in situ by rhodium acetate catalyzed decomposition of N-(diazoacetyl)-N-methylalkynamide derivatives 16a-c, 18c, and 18d have been studied.The intermediate cycloadducts fragmentate spontaneously under the reaction conditions (110 deg C) to afford the annulated furans 19a-c, 20c, and 20d. - Keywords: Carbonyl ylides; Furans; Intramolecular cycloadditions; Isomuenchnones

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