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methyl 2-carboxybenzofuran-3-acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76268-17-2

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  • 76268-17-2 Structure
  • Basic information

    1. Product Name: methyl 2-carboxybenzofuran-3-acetate
    2. Synonyms:
    3. CAS NO:76268-17-2
    4. Molecular Formula:
    5. Molecular Weight: 234.208
    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: methyl 2-carboxybenzofuran-3-acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 2-carboxybenzofuran-3-acetate(76268-17-2)
    11. EPA Substance Registry System: methyl 2-carboxybenzofuran-3-acetate(76268-17-2)
  • 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: 76268-17-2(Hazardous Substances Data)

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76268-17-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76268-17-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,2,6 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 76268-17:
(7*7)+(6*6)+(5*2)+(4*6)+(3*8)+(2*1)+(1*7)=152
152 % 10 = 2
So 76268-17-2 is a valid CAS Registry Number.

76268-17-2Downstream Products

76268-17-2Relevant academic research and scientific papers

Furo[3,4-b]benzofurans: Synthesis and reactions

Traulsen, Tim,Friedrichsen, Willy

, p. 1387 - 1398 (2000)

Starting with coumarin (1) furo[3,4-b]benzofuran 4 was synthesized using the Hamaguchi-Ibata methodology. Intermolecular Diels-Alder reactions provide compounds 5-8. In a [4 + 3] cycloaddition reaction with oxyallyl compound 9 was obtained. The C-annulated furans 16a (in situ) and 16b have been prepared by a similar methodology starting with 10a,b. In an intramolecular Diels-Alder reaction compounds 17a,b were obtained. Computational studies concerning the reactivity of furo[3,4-b]benzofurans in inter- and intramolecular Diels-Alder reactions using both semiempirical (AM1, PM3) and density functional theoretical methods (B3LYP/6-31G*) are reported.

Syntheses of Furano Compounds: Part XLIV. Syntheses of 2-CarboxybenzoFuran-3-Acetic Acid and 3-CarboxybenzoFuran-2-Acetic Acid

Chatterjea, J. N.,Sahai, Radhika Pati

, p. 633 - 636 (2007/10/02)

1-Carboxybenzofuran-3-acetic acid and 3-carboxybenzofuran-acetic acid have been synthesised. A new synthesis of benzofuran-3-acetic acid, a plant hormone is reported.

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