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ethyl 4-chloro-4-(4-chlorophenylthio)butanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 146564-01-4 Structure
  • Basic information

    1. Product Name: ethyl 4-chloro-4-(4-chlorophenylthio)butanoate
    2. Synonyms: ethyl 4-chloro-4-(4-chlorophenylthio)butanoate
    3. CAS NO:146564-01-4
    4. Molecular Formula:
    5. Molecular Weight: 293.214
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 146564-01-4.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: ethyl 4-chloro-4-(4-chlorophenylthio)butanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 4-chloro-4-(4-chlorophenylthio)butanoate(146564-01-4)
    11. EPA Substance Registry System: ethyl 4-chloro-4-(4-chlorophenylthio)butanoate(146564-01-4)
  • 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: 146564-01-4(Hazardous Substances Data)

146564-01-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146564-01-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,5,6 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 146564-01:
(8*1)+(7*4)+(6*6)+(5*5)+(4*6)+(3*4)+(2*0)+(1*1)=134
134 % 10 = 4
So 146564-01-4 is a valid CAS Registry Number.

146564-01-4Relevant articles and documents

Lewis acid-promoted alkylations of arenes and 1-trimethylsilylalkynes with β-chloro-β-thiopropanoic esters

Ishibashi,Mino,Sakata,Inada,Ikeda

, p. 1148 - 1151 (2007/10/02)

Ethyl 3-chloro-3-(3,4-dichlorophenylthio)propanoate (8) reacted with electron-rich arenes in the presence of titanium tetrachloride to give the Friedel-Crafts products 10a-13a. Reactions of 8 with 1-trimethylsilylalkynes 14a-d were effected with aluminum chloride to afford the substitution products 15a-d. Some chemical transformations of the products are also described.

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