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22905-10-8

1-ethyl-4-(ethylthio)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 22905-10-8 Structure

  • Basic information

    1. Product Name: 1-ethyl-4-(ethylthio)benzene
    2. Synonyms: 1-ethyl-4-(ethylthio)benzene
    3. CAS NO:22905-10-8
    4. Molecular Formula:
    5. Molecular Weight: 166.287
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 22905-10-8.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-ethyl-4-(ethylthio)benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-ethyl-4-(ethylthio)benzene(22905-10-8)
    11. EPA Substance Registry System: 1-ethyl-4-(ethylthio)benzene(22905-10-8)

  • 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: 22905-10-8(Hazardous Substances Data)

22905-10-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22905-10-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,0 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22905-10:
(7*2)+(6*2)+(5*9)+(4*0)+(3*5)+(2*1)+(1*0)=88
88 % 10 = 8
So 22905-10-8 is a valid CAS Registry Number.

22905-10-8Relevant articles and documents

Metallation reactions. XXI. Metallation of alkyl (alkylthio) benzenes by superbases versus organolithium compounds

Cabiddu, Salvatore,Fattuoni, Claudia,Floris, Costantino,Melis, Stefana,Serci, Alessandro

, p. 6037 - 6048 (1994)

The metallation regiochemistry of alkyl(alkylthio)benzenes with butyllithium or with the superbasic mixture of butyllithium with potassium tert-butoxide is described. The reaction pattern depends on the substrate and the reagent. Butyllithium monometallates the thiomethylic carbon of methyl (methylthio) benzenes and bimetallates the thiomethylic and the annular carbon ortho to the thioethereal group. With superbases the metallation occurs at the thiomethylic and methylic carbon. Metallation with butyllithium of the higher homologs substitutes exclusively the hydrogen ortho to the thioalkylic group, while the superbases attack also the carbon atom alpha to the thioalkyl substituent.

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