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CAS

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1356628-47-1

9,14-diphenyl-12-(trimethylsilyl)benzo[f]tetraphen-11-yl trifluoromethanesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1356628-47-1 Structure

  • Basic information

    1. Product Name: 9,14-diphenyl-12-(trimethylsilyl)benzo[f]tetraphen-11-yl trifluoromethanesulfonate
    2. Synonyms: 9,14-diphenyl-12-(trimethylsilyl)benzo[f]tetraphen-11-yl trifluoromethanesulfonate
    3. CAS NO:1356628-47-1
    4. Molecular Formula:
    5. Molecular Weight: 650.793
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1356628-47-1.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: 9,14-diphenyl-12-(trimethylsilyl)benzo[f]tetraphen-11-yl trifluoromethanesulfonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9,14-diphenyl-12-(trimethylsilyl)benzo[f]tetraphen-11-yl trifluoromethanesulfonate(1356628-47-1)
    11. EPA Substance Registry System: 9,14-diphenyl-12-(trimethylsilyl)benzo[f]tetraphen-11-yl trifluoromethanesulfonate(1356628-47-1)

  • 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: 1356628-47-1(Hazardous Substances Data)

1356628-47-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1356628-47-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,6,6,2 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1356628-47:
(9*1)+(8*3)+(7*5)+(6*6)+(5*6)+(4*2)+(3*8)+(2*4)+(1*7)=181
181 % 10 = 1
So 1356628-47-1 is a valid CAS Registry Number.

1356628-47-1Relevant articles and documents

Straightforward Synthesis of Novel Acene-Based Aryne Precursors

Rodríguez-Lojo, Diego,Pe?a, Diego,Pérez, Dolores,Guitián, Enrique

, p. 1633 - 1637 (2015)

Large polycyclic o-(trimethylsilyl)aryl triflates are easily obtained by reaction of commercially available bisaryne precursors with cyclopentadienones. The transformation involves controlled generation of one of the aryne functionalities, trapping by Die

Cloverphene: A Clover-Shaped cata-Condensed Nanographene with Sixteen Fused Benzene Rings

Alonso, Jose M.,Diaz-Alvarez, Alba E.,Criado, Alejandro,Perez, Dolores,Pena, Diego,Guitian, Enrique

, p. 173 - 177 (2012/03/26)

Living in clover: Sequential [4+2] and [2+2+2] aryne cycloadditions allow the isolation of cloverlike and archlike nanographenes (see picture). This approach led to the synthesis of the largest cata-condensed aromatic hydrocarbon that has been obtained to date, a system formed by 16 fused benzene rings (22 benzene rings in total) and 102 sp2 carbon atoms.

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