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1409941-01-0

3-octyl-2-(9H-xanthen-9-yl)-3H-inden-5-yl-4-methylbenzenesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1409941-01-0 Structure

  • Basic information

    1. Product Name: 3-octyl-2-(9H-xanthen-9-yl)-3H-inden-5-yl-4-methylbenzenesulfonate
    2. Synonyms: 3-octyl-2-(9H-xanthen-9-yl)-3H-inden-5-yl-4-methylbenzenesulfonate
    3. CAS NO:1409941-01-0
    4. Molecular Formula:
    5. Molecular Weight: 578.772
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1409941-01-0.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: 3-octyl-2-(9H-xanthen-9-yl)-3H-inden-5-yl-4-methylbenzenesulfonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-octyl-2-(9H-xanthen-9-yl)-3H-inden-5-yl-4-methylbenzenesulfonate(1409941-01-0)
    11. EPA Substance Registry System: 3-octyl-2-(9H-xanthen-9-yl)-3H-inden-5-yl-4-methylbenzenesulfonate(1409941-01-0)

  • 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: 1409941-01-0(Hazardous Substances Data)

1409941-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1409941-01-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,9,9,4 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1409941-01:
(9*1)+(8*4)+(7*0)+(6*9)+(5*9)+(4*4)+(3*1)+(2*0)+(1*1)=160
160 % 10 = 0
So 1409941-01-0 is a valid CAS Registry Number.

1409941-01-0Downstream Products

1409941-01-0Relevant articles and documents

TfOH/Fe(OTf)3 Cocatalyzed Reaction of Arylallenes with Alcohols for Structurally Diverse Indene Derivatives

Liu, Congrong,Zhang, Haiyun,Ding, Lianghui,Liu, Juan

, p. 737 - 742 (2018/07/29)

The indene moiety is an important unit because of its presence in many chemical catalysts, functional materials and biologically relevant molecules. Herein, we report a facile reaction of arylallenes with benzylic or allylic alcohols through TfOH/Fe(OTf)3 cocatalyzed cleavage of sp3 carbon-oxygen. In the presence of 5 mol% TfOH and 5 mol% Fe(OTf)3, a range of arylallenes undergo carbocation initiated cyclization reaction with alkyl alcohols to give structurally diverse polysubstituted indenes in good to excellent yields. H2O is the sole byproduct that makes this transformation highly atom-economic and environmentally benign.

Ferric chloride-catalyzed C-N bond cleavage for the cyclization of arylallenes leading to polysubstituted indenes

Liu, Cong-Rong,Wang, Ting-Ting,Qi, Qing-Biao,Tian, Shi-Kai

, p. 10913 - 10915 (2012/11/07)

A range of arylallenes undergo carbocation-initiated cyclization reaction with N-benzylic and N-allylic sulfonamides in the presence of 10 mol% ferric chloride to give structurally diverse polysubstituted indenes in good yields with extremely high regioselectivity.

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