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2-(4-Methoxy-phenylamino)-N-phenyl-2-thioxo-acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 125983-66-6 Structure
  • Basic information

    1. Product Name: 2-(4-Methoxy-phenylamino)-N-phenyl-2-thioxo-acetamide
    2. Synonyms:
    3. CAS NO:125983-66-6
    4. Molecular Formula:
    5. Molecular Weight: 286.354
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 125983-66-6.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-(4-Methoxy-phenylamino)-N-phenyl-2-thioxo-acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-Methoxy-phenylamino)-N-phenyl-2-thioxo-acetamide(125983-66-6)
    11. EPA Substance Registry System: 2-(4-Methoxy-phenylamino)-N-phenyl-2-thioxo-acetamide(125983-66-6)
  • 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: 125983-66-6(Hazardous Substances Data)

125983-66-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125983-66-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,9,8 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 125983-66:
(8*1)+(7*2)+(6*5)+(5*9)+(4*8)+(3*3)+(2*6)+(1*6)=156
156 % 10 = 6
So 125983-66-6 is a valid CAS Registry Number.

125983-66-6Relevant articles and documents

Dithiocarboxylic Acids, Dithiocarboxylic Esters, or Thiocarboxylic Amides by Reaction of Methylene-active Chloromethyl Compounds with Sulfur

Thiel, W.,Mayer, R.

, p. 243 - 262 (2007/10/02)

With a mixture of sulfur and amine in DMF at room temperature halomethyl compounds (1,5-10) can be oxidized to give thiocarboxylic acids (2,11-16) and their derivatives (3,4,17-35).We studied this reaction in detail especially with chloroacetic derivatives (11-15) or chloromethyl heterocycles (16) formally derived from chloroacetic acid.The resulting thiooxalic acid derivatives (11-27) represent activated acids and very useful C2-synthons, especially for the synthesis of heterocycles.Oxidation in the presence of triethylamine leads to dithiocarboxylates (11-16) which can be alkylated to dithioesters (17-27) in high yields.As a rule, with different primary and secondary amines instead of tertiary amines these dithiocarboxylates or dithiocarboxylic esters can be transformed already at low temperatures to thioamides (28-35).

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