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2-(4-methyl)phenyl-6-methylbenzothiophene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22720-97-4

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  • 22720-97-4 Structure
  • Basic information

    1. Product Name: 2-(4-methyl)phenyl-6-methylbenzothiophene
    2. Synonyms: 2-(4-methyl)phenyl-6-methylbenzothiophene
    3. CAS NO:22720-97-4
    4. Molecular Formula:
    5. Molecular Weight: 238.353
    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-(4-methyl)phenyl-6-methylbenzothiophene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-methyl)phenyl-6-methylbenzothiophene(22720-97-4)
    11. EPA Substance Registry System: 2-(4-methyl)phenyl-6-methylbenzothiophene(22720-97-4)
  • 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: 22720-97-4(Hazardous Substances Data)

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22720-97-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22720-97-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,7,2 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22720-97:
(7*2)+(6*2)+(5*7)+(4*2)+(3*0)+(2*9)+(1*7)=94
94 % 10 = 4
So 22720-97-4 is a valid CAS Registry Number.

22720-97-4Downstream Products

22720-97-4Relevant academic research and scientific papers

Phthalimidesulfenyl chloride; part VII: Synthesis of 2-substituted 3-chlorobenzo[b]thiophenes and related heteroaromatics

Capozzi,De Sio,Menichetti,Nativi,Pacini

, p. 521 - 525 (2007/10/02)

Addition of phthalimidesulfenyl chloride (1) to diaryl- or alkyl(aryl) acetylenes affords (E)-β-chlorovinylsulfenamides 3. These species react with aluminum trichloride and other Lewis acids to give benzo[b]thiophenes 6 through an intramolecular electrophilic substitution. The reaction is very simple and seems insensitive to the nature of substituents at the double bond of vinylsulfenamides 3. Following the same strategy the thienothiophene 11 and the condensed thiopyran 12 were also prepared.

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