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2-N-methylanilinoacetylbenzofuran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76007-18-6

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  • 76007-18-6 Structure

  • Basic information

    1. Product Name: 2-N-methylanilinoacetylbenzofuran
    2. Synonyms: 2-N-methylanilinoacetylbenzofuran
    3. CAS NO:76007-18-6
    4. Molecular Formula:
    5. Molecular Weight: 265.312
    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-N-methylanilinoacetylbenzofuran(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-N-methylanilinoacetylbenzofuran(76007-18-6)
    11. EPA Substance Registry System: 2-N-methylanilinoacetylbenzofuran(76007-18-6)

  • 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: 76007-18-6(Hazardous Substances Data)

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76007-18-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76007-18-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,0 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76007-18:
(7*7)+(6*6)+(5*0)+(4*0)+(3*7)+(2*1)+(1*8)=116
116 % 10 = 6
So 76007-18-6 is a valid CAS Registry Number.

76007-18-6Relevant academic research and scientific papers

Light-induced Reactions of Heteroaryl N-Methylanilinomethyl Ketones: Formation of 3-Heteroaryl-1-phenylazetidin-3-ols

Hesabi, Massoud M.,Hill, John,El-Hamamy, Ahmad A.

, p. 2371 - 2373 (2007/10/02)

A series of heteroaryl N-methylanilinomethyl ketones, PhNMe*CH2COR (R=heteroaryl), were irradiated with ether as the solvent.The corresponding 3-heteroaryl-1-phenylazetidin-3-ols (type II cyclisation products) were formed when R was 2-furyl, benzofuran-2-yl, 2-thienyl, 1-methylpyrrol-2-yl, and 2,4-dimethylthiazol-5-yl, but such products were not isolated when R was pyrrol-2-yl or 3-pyridyl.In some cases, products formed via type II fission were obtained.

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