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270588-43-7

3-(3-bromo-2-methoxy-phenyl)-3H-benzofuran-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 270588-43-7 Structure

  • Basic information

    1. Product Name: 3-(3-bromo-2-methoxy-phenyl)-3H-benzofuran-2-one
    2. Synonyms: 3-(3-bromo-2-methoxy-phenyl)-3H-benzofuran-2-one
    3. CAS NO:270588-43-7
    4. Molecular Formula:
    5. Molecular Weight: 319.155
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 270588-43-7.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: 3-(3-bromo-2-methoxy-phenyl)-3H-benzofuran-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(3-bromo-2-methoxy-phenyl)-3H-benzofuran-2-one(270588-43-7)
    11. EPA Substance Registry System: 3-(3-bromo-2-methoxy-phenyl)-3H-benzofuran-2-one(270588-43-7)

  • 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: 270588-43-7(Hazardous Substances Data)

270588-43-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 270588-43-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,0,5,8 and 8 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 270588-43:
(8*2)+(7*7)+(6*0)+(5*5)+(4*8)+(3*8)+(2*4)+(1*3)=157
157 % 10 = 7
So 270588-43-7 is a valid CAS Registry Number.

270588-43-7Relevant articles and documents

Progress toward synthesis of diazonamide A. Preparation of a 3-(oxazol-5-yl)-4-trifluoromethyl-sulfonyloxyindole and its use in biaryl coupling reactions

Vedejs, Edwin,Barda, David A.

, p. 1033 - 1035 (2007/10/03)

The synthesis of a 3-oxazol-5-yl-indole-4-triflate is described, featuring a Schoelkopf reaction to prepare the oxazole. In addition, the participation of this intermediate in biaryl coupling reactions toward the total synthesis of the natural product dia

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