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2-(1,1-Bis-phenylsulfanyl-ethyl)-5-methoxy-benzo[1,3]oxathiole 3,3-dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 181510-05-4 Structure
  • Basic information

    1. Product Name: 2-(1,1-Bis-phenylsulfanyl-ethyl)-5-methoxy-benzo[1,3]oxathiole 3,3-dioxide
    2. Synonyms: 2-(1,1-Bis-phenylsulfanyl-ethyl)-5-methoxy-benzo[1,3]oxathiole 3,3-dioxide
    3. CAS NO:181510-05-4
    4. Molecular Formula:
    5. Molecular Weight: 444.596
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 181510-05-4.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: 2-(1,1-Bis-phenylsulfanyl-ethyl)-5-methoxy-benzo[1,3]oxathiole 3,3-dioxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(1,1-Bis-phenylsulfanyl-ethyl)-5-methoxy-benzo[1,3]oxathiole 3,3-dioxide(181510-05-4)
    11. EPA Substance Registry System: 2-(1,1-Bis-phenylsulfanyl-ethyl)-5-methoxy-benzo[1,3]oxathiole 3,3-dioxide(181510-05-4)
  • 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: 181510-05-4(Hazardous Substances Data)

181510-05-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 181510-05-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,5,1 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 181510-05:
(8*1)+(7*8)+(6*1)+(5*5)+(4*1)+(3*0)+(2*0)+(1*5)=104
104 % 10 = 4
So 181510-05-4 is a valid CAS Registry Number.

181510-05-4Relevant articles and documents

Sulfogriseofulvin derivatives. Synthesis by [4+2]cycloaddition, structure, properties, crystal structure analysis, and antifungal activity of spiro[1,3-benzoxathiole-2,1'-cyclohex-2'-en]-4'-one 3,3-dioxides

Friedrich, Michael,Meichle, Wilhelm,Bernhard, Harald,Rihs, Grety,Otto, Hans-Hartwig

, p. 361 - 370 (1996)

Syntheses of substituted, especially of fluoro substituted benzoxathiole 1,1-dioxides, are described. These derivatives were transformed via the Peterson olefination into substituted 2-alkylidene derivatives 27. Diels-Alder reactions of 27 with 1,1-dimeth

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