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143582-17-6

3(2H)-Benzofuranone, 2-benzoyl-5-chloro-6-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 143582-17-6 Structure

  • Basic information

    1. Product Name: 3(2H)-Benzofuranone, 2-benzoyl-5-chloro-6-methyl-
    2. Synonyms:
    3. CAS NO:143582-17-6
    4. Molecular Formula: C16H11ClO3
    5. Molecular Weight: 286.715
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 143582-17-6.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(2H)-Benzofuranone, 2-benzoyl-5-chloro-6-methyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3(2H)-Benzofuranone, 2-benzoyl-5-chloro-6-methyl-(143582-17-6)
    11. EPA Substance Registry System: 3(2H)-Benzofuranone, 2-benzoyl-5-chloro-6-methyl-(143582-17-6)

  • 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: 143582-17-6(Hazardous Substances Data)

143582-17-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143582-17-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,5,8 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 143582-17:
(8*1)+(7*4)+(6*3)+(5*5)+(4*8)+(3*2)+(2*1)+(1*7)=126
126 % 10 = 6
So 143582-17-6 is a valid CAS Registry Number.

143582-17-6Downstream Products

143582-17-6Relevant articles and documents

A new synthesis of 2-aroylcoumaran-3-ones by hypervalent iodine oxidation of 2-acetyl-phenyl benzoates using [hydroxy(tosyloxy)iodo]benzene

Prakash,Goyal

, p. 629 - 630 (1992)

Hypervalent iodine oxidation of 2-acetylphenyl benzoates 1 a-f using [hydroxy(tosyloxy)iodo]benzene (HTIB), followed by Baker-Venkatraman rearrangement of the resultant 2-[(tosyloxy)acetylphenyl benzoates 2a-f with potassium hydroxide, provides a new conv

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