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532931-56-9

Acetamide, 2,2,2-trifluoro-N-[(4-nitrophenyl)thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 532931-56-9 Structure

  • Basic information

    1. Product Name: Acetamide, 2,2,2-trifluoro-N-[(4-nitrophenyl)thio]-
    2. Synonyms:
    3. CAS NO:532931-56-9
    4. Molecular Formula: C8H5F3N2O3S
    5. Molecular Weight: 266.201
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 532931-56-9.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: Acetamide, 2,2,2-trifluoro-N-[(4-nitrophenyl)thio]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetamide, 2,2,2-trifluoro-N-[(4-nitrophenyl)thio]-(532931-56-9)
    11. EPA Substance Registry System: Acetamide, 2,2,2-trifluoro-N-[(4-nitrophenyl)thio]-(532931-56-9)

  • 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: 532931-56-9(Hazardous Substances Data)

532931-56-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 532931-56-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,2,9,3 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 532931-56:
(8*5)+(7*3)+(6*2)+(5*9)+(4*3)+(3*1)+(2*5)+(1*6)=149
149 % 10 = 9
So 532931-56-9 is a valid CAS Registry Number.

532931-56-9Relevant articles and documents

Efficient synthesis of N-acylarenesulfenamides by acylation of arenesulfenamides

Bao, Ming,Shimizu, Masao,Shimada, Shigeru,Tanaka, Masato

, p. 303 - 309 (2007/10/03)

Acylation of arenesulfenamides proceeds efficiently by using either perfluorocarboxylic anhydrides or acid chlorides in the presence of pyridine as a base at low temperatures to give N-acylarenesulfenamides. Some N-alkylcarbonyl derivatives exist with imidic acid tautomers in an aprotic solvent.

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