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260547-98-6

4-methylphenyl 1-(methylsulfanyl)-1-propenyl sulfone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 260547-98-6 Structure

  • Basic information

    1. Product Name: 4-methylphenyl 1-(methylsulfanyl)-1-propenyl sulfone
    2. Synonyms: 4-methylphenyl 1-(methylsulfanyl)-1-propenyl sulfone
    3. CAS NO:260547-98-6
    4. Molecular Formula: C11H14O2S2
    5. Molecular Weight: 242.35766
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 260547-98-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-methylphenyl 1-(methylsulfanyl)-1-propenyl sulfone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-methylphenyl 1-(methylsulfanyl)-1-propenyl sulfone(260547-98-6)
    11. EPA Substance Registry System: 4-methylphenyl 1-(methylsulfanyl)-1-propenyl sulfone(260547-98-6)

  • 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: 260547-98-6(Hazardous Substances Data)

260547-98-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 260547-98-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,0,5,4 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 260547-98:
(8*2)+(7*6)+(6*0)+(5*5)+(4*4)+(3*7)+(2*9)+(1*8)=146
146 % 10 = 6
So 260547-98-6 is a valid CAS Registry Number.

260547-98-6Relevant articles and documents

Heterocyclic synthesis by C-C bond formation. Thionium ion-mediated preparation of substituted pyrrolidines and piperidines

Craig, Donald,Meadows, James D.,Pecheux, Muriel

, p. 147 - 150 (2007/10/03)

Dithioacetal-S,S-dioxides 6 and 7 undergo cyclisation to give pyrrolidines and piperidines upon exposure to Lewis acid. An unexpected tandem cyclisation of 5 to give 10 is described.

Radical-induced 1,3-Rearrangemets of Allylic Sulfones bearing an Alkylthio or Arylthio Substituent at the α-Position

Fox, Judith M.,Morris, Clare M.,Smyth, G. Darren,Whitman, Gordon H.

, p. 731 - 738 (2007/10/02)

1-Methylthio-1-p-tolylsulfonylprop-2-ene 2 underwent 1,3-rearrangement under conditions of radical initiation with migration of the p-tolylsulfonyl group by a process considered to have involved addition-elimination of arylsulfonyl radicals.In contrast, t

A Facile Allylic 1,3-Rearrangement of a Sulfonyl Group and Its Application to a Synthesis of α,β-Unsaturated Ketones

Ogura, Katsuyuki,Iihama, Teruyuki,Kiuchi, Shigeo,Kajiki, Toshitaka,Koshikawa, Osamu,et al.

, p. 700 - 705 (2007/10/02)

A p-tolylsulfonyl group undergoes a SiO2-catalyzed 1,3-rearrangement in a sulfenylated allylic system and this rearrangement can be utylized in novel and convenient syntheses of α,β-unsaturated ketones 6 using 3-(methylthio)-2-propenyl p-tolyl sulfone (1)

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