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102469-09-0

2-biphenyl-4-yl-3-methyl-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 102469-09-0 Structure

  • Basic information

    1. Product Name: 2-biphenyl-4-yl-3-methyl-indole
    2. Synonyms: 2-biphenyl-4-yl-3-methyl-indole
    3. CAS NO:102469-09-0
    4. Molecular Formula:
    5. Molecular Weight: 283.373
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 102469-09-0.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: 2-biphenyl-4-yl-3-methyl-indole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-biphenyl-4-yl-3-methyl-indole(102469-09-0)
    11. EPA Substance Registry System: 2-biphenyl-4-yl-3-methyl-indole(102469-09-0)

  • 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: 102469-09-0(Hazardous Substances Data)

102469-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102469-09-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,4,6 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 102469-09:
(8*1)+(7*0)+(6*2)+(5*4)+(4*6)+(3*9)+(2*0)+(1*9)=100
100 % 10 = 0
So 102469-09-0 is a valid CAS Registry Number.

102469-09-0Downstream Products

102469-09-0Relevant articles and documents

Synthesis of Ester-Substituted Indolo[2,1-a]isoquinolines via Photocatalyzed Alkoxycarbonylation/Cyclization Reactions

Chen, Jian-Qiang,Tu, Xiaodong,Qin, Binyan,Huang, Shaoxin,Zhang, Jun,Wu, Jie

supporting information, p. 642 - 647 (2022/01/20)

A direct alkoxycarbonylation/cyclization reaction is accomplished under visible light-induced photoredox catalysis. With this approach, a variety of ester-substituted indolo[2,1-a]isoquinolines are prepared in good to excellent yields. It is worth noting that this method not only can afford the synthesis of indolo[2,1-a]isoquinolines but also can provide an alternative route for generating complex target structures bearing carboxylic esters.

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