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CAS

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1266329-38-7

N-methyl-2-{[2-(phenylethynyl)phenyl]ethynyl}aniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1266329-38-7 Structure

  • Basic information

    1. Product Name: N-methyl-2-{[2-(phenylethynyl)phenyl]ethynyl}aniline
    2. Synonyms: N-methyl-2-{[2-(phenylethynyl)phenyl]ethynyl}aniline
    3. CAS NO:1266329-38-7
    4. Molecular Formula:
    5. Molecular Weight: 307.395
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1266329-38-7.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: N-methyl-2-{[2-(phenylethynyl)phenyl]ethynyl}aniline(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-methyl-2-{[2-(phenylethynyl)phenyl]ethynyl}aniline(1266329-38-7)
    11. EPA Substance Registry System: N-methyl-2-{[2-(phenylethynyl)phenyl]ethynyl}aniline(1266329-38-7)

  • 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: 1266329-38-7(Hazardous Substances Data)

1266329-38-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1266329-38-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,6,3,2 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1266329-38:
(9*1)+(8*2)+(7*6)+(6*6)+(5*3)+(4*2)+(3*9)+(2*3)+(1*8)=167
167 % 10 = 7
So 1266329-38-7 is a valid CAS Registry Number.

1266329-38-7Downstream Products

1266329-38-7Relevant articles and documents

Direct synthesis of fused indoles by gold-catalyzed cascade cyclization of diynes

Hirano, Kimio,Inaba, Yusuke,Takahashi, Naoya,Shimano, Masanao,Oishi, Shinya,Fujii, Nobutaka,Ohno, Hiroaki

experimental part, p. 1212 - 1227 (2011/04/25)

A direct, concise, and atom-economical synthetic method for the generation of fused indoles, using a gold-catalyzed cascade cyclization of diynes, has been developed. The reaction gave various fused indoles, such as aryl-annulated[a]carbazoles, dihydrobenzo[g]indoles, and azepino-or oxepinoindole derivatives in good to excellent yields, through an intramolecular cascade 5-endo-dig hydroamination followed by a 6-or 7-endo-dig cycloisomerization, without producing theoretical byproduct. Three of the resulting indoles exhibited potent antifungal activities against T. mentagrophytes and T. rubrum, demonstrating the practical application of the described cascade reaction for drug discovery.(Figure Presented)

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