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82883-69-0

5,6,7,8-tetrahydro-1-p-tolyl-2,4-diphenylquinolinium trifluoromethanesulphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 5,6,7,8-tetrahydro-1-p-tolyl-2,4-diphenylquinolinium trifluoromethanesulphonate

    Cas No: 82883-69-0

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  • 82883-69-0 Structure

  • Basic information

    1. Product Name: 5,6,7,8-tetrahydro-1-p-tolyl-2,4-diphenylquinolinium trifluoromethanesulphonate
    2. Synonyms: 5,6,7,8-tetrahydro-1-p-tolyl-2,4-diphenylquinolinium trifluoromethanesulphonate
    3. CAS NO:82883-69-0
    4. Molecular Formula:
    5. Molecular Weight: 525.592
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 82883-69-0.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: 5,6,7,8-tetrahydro-1-p-tolyl-2,4-diphenylquinolinium trifluoromethanesulphonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5,6,7,8-tetrahydro-1-p-tolyl-2,4-diphenylquinolinium trifluoromethanesulphonate(82883-69-0)
    11. EPA Substance Registry System: 5,6,7,8-tetrahydro-1-p-tolyl-2,4-diphenylquinolinium trifluoromethanesulphonate(82883-69-0)

  • 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: 82883-69-0(Hazardous Substances Data)

82883-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82883-69-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,8,8 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 82883-69:
(7*8)+(6*2)+(5*8)+(4*8)+(3*3)+(2*6)+(1*9)=170
170 % 10 = 0
So 82883-69-0 is a valid CAS Registry Number.

82883-69-0Relevant articles and documents

Nucleophilic Displacements of N-Aryl and Heteroaryl Groups. Part 1. Pyrylium-mediated Transformation of Anilines into Phenols

Katritzky, Alan R.,Langthorne, Ronald T.,Muathin, Hussni A.,Patel, Ranjian C.

, p. 2601 - 2604 (2007/10/02)

Aromatic amines with 2,4-diphenyl-5,6,7,8-tetrahydrochromenylium trifluoromethanesulphonate (5) gave the corresponding pyridinium salts (6; R = aryl) which were converted by base into the anhydrobases (7).Benzoyl chloride converted (7) into the new pyridinium anhydrobases (9).These anhydrobases (9) rearrangement at 150 deg C into the isomeric phenol enol ethers (10) which were readily hydrolysed to yield the corresponding phenols.The mechanistic and synthetic significance of the results are assessed.

The Chemistry of Some Bicyclic Pyridinium Anhydrobases

Katritzky, Alan R.,Ueroegdi, Laszlo,Patel, Ranjan C.

, p. 1349 - 1354 (2007/10/02)

The anhydrobase from 5,6,7,8-tetrahydro-2,4-diphenyl-1-p-tolylquinolinium reacts with C-, N-, and S-electrophiles to form adducts and new anhydrobases.The tautomeric structures of the adducts are deduced from spectral evidence.

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