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1146473-28-0

9-benzyl-3-(1-benzyl-5-fluoro-1H-indol-2-yl)-6-fluoro-2,3,4,9-tetrahydro-1H-carbazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1146473-28-0 Structure

  • Basic information

    1. Product Name: 9-benzyl-3-(1-benzyl-5-fluoro-1H-indol-2-yl)-6-fluoro-2,3,4,9-tetrahydro-1H-carbazole
    2. Synonyms: 9-benzyl-3-(1-benzyl-5-fluoro-1H-indol-2-yl)-6-fluoro-2,3,4,9-tetrahydro-1H-carbazole
    3. CAS NO:1146473-28-0
    4. Molecular Formula:
    5. Molecular Weight: 502.607
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1146473-28-0.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: 9-benzyl-3-(1-benzyl-5-fluoro-1H-indol-2-yl)-6-fluoro-2,3,4,9-tetrahydro-1H-carbazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9-benzyl-3-(1-benzyl-5-fluoro-1H-indol-2-yl)-6-fluoro-2,3,4,9-tetrahydro-1H-carbazole(1146473-28-0)
    11. EPA Substance Registry System: 9-benzyl-3-(1-benzyl-5-fluoro-1H-indol-2-yl)-6-fluoro-2,3,4,9-tetrahydro-1H-carbazole(1146473-28-0)

  • 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: 1146473-28-0(Hazardous Substances Data)

1146473-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1146473-28-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,6,4,7 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1146473-28:
(9*1)+(8*1)+(7*4)+(6*6)+(5*4)+(4*7)+(3*3)+(2*2)+(1*8)=150
150 % 10 = 0
So 1146473-28-0 is a valid CAS Registry Number.

1146473-28-0Downstream Products

1146473-28-0Relevant articles and documents

Chalcogen???π Bonding Catalysis

Kong, Xiangjin,Zhou, Pan-Pan,Wang, Yao

, p. 9395 - 9400 (2021)

While the presence of sulfur???π bonding interaction is a general phenomenon in the biological systems, the exploitation of this noncovalent force in a chemical process yet remains elusive. Herein, we describe the concept of chalcogen???π bonding catalysis that activates molecules of π systems through the interaction between chalcogen and π-electron cloud. The proof-of-concept studies using a vinylindole-based Diels–Alder benchmark reaction demonstrate that S???π and Se???π bonding interaction can drive the cycloaddition reaction efficiently. Experimental results suggest that a simultaneously double Se???π bonding interaction directs the stereoselectivity in this cycloaddition process.

Bronsted acid mediated tandem diels-alder/ aromatization reactions of vinylindoles

Chen, Cai-Bao,Wang, Xu-Fan,Cao, Yi-Ju,Cheng, Hong-Gang,Xiao, Wen-Jing

supporting information; experimental part, p. 3532 - 3535 (2009/09/30)

A Bronsted acid catalyzed tandem Diels - Alder/aromatiza-tion reaction of 2-vinylindoles has been developed. The reaction provides a highly efficient and concise approach to 3-indolyl-substituted tetrahydrocarbazoles with various substituents in high yiel

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