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CAS

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98088-09-6

1-(methylthio)-2-<4-cyanobenzyl>naphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 98088-09-6 Structure

  • Basic information

    1. Product Name: 1-(methylthio)-2-<4-cyanobenzyl>naphthalene
    2. Synonyms:
    3. CAS NO:98088-09-6
    4. Molecular Formula:
    5. Molecular Weight: 289.401
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 98088-09-6.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: 1-(methylthio)-2-<4-cyanobenzyl>naphthalene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(methylthio)-2-<4-cyanobenzyl>naphthalene(98088-09-6)
    11. EPA Substance Registry System: 1-(methylthio)-2-<4-cyanobenzyl>naphthalene(98088-09-6)

  • 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: 98088-09-6(Hazardous Substances Data)

98088-09-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98088-09-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,0,8 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 98088-09:
(7*9)+(6*8)+(5*0)+(4*8)+(3*8)+(2*0)+(1*9)=176
176 % 10 = 6
So 98088-09-6 is a valid CAS Registry Number.

98088-09-6Downstream Products

98088-09-6Relevant articles and documents

Photochemical Conversion of Sulfonium Salts via a 1,3-Sigmatropic Rearrangement. Photogeneration of Broensted Acids

Saeva, Franklin D.,Morgan, Bradley P.,Luss, Henry R.

, p. 4360 - 4362 (1985)

A series of 1-naphthyl methyl-substituted alkylsulfonium salts underwent 1,3-sigmatropic rearrangements to form 1-(methylthio)-2-substituted alkylnaphthalenes and the corresponding acid with quantum yields between 0.24 and 0.10.In competition with rearrangement was a bond-cleavage reaction forming 1-naphthyl methyl sulfide.The quantum yield for bond cleavage was ca. 0.15 for all the compounds studied.

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