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3-cyclohexyl-2-(2-pyridylsulfanyl)-propionamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 189809-76-5 Structure
  • Basic information

    1. Product Name: 3-cyclohexyl-2-(2-pyridylsulfanyl)-propionamide
    2. Synonyms: 3-cyclohexyl-2-(2-pyridylsulfanyl)-propionamide
    3. CAS NO:189809-76-5
    4. Molecular Formula:
    5. Molecular Weight: 264.392
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 189809-76-5.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: 3-cyclohexyl-2-(2-pyridylsulfanyl)-propionamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-cyclohexyl-2-(2-pyridylsulfanyl)-propionamide(189809-76-5)
    11. EPA Substance Registry System: 3-cyclohexyl-2-(2-pyridylsulfanyl)-propionamide(189809-76-5)
  • 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: 189809-76-5(Hazardous Substances Data)

189809-76-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 189809-76-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,8,0 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 189809-76:
(8*1)+(7*8)+(6*9)+(5*8)+(4*0)+(3*9)+(2*7)+(1*6)=205
205 % 10 = 5
So 189809-76-5 is a valid CAS Registry Number.

189809-76-5Downstream Products

189809-76-5Relevant articles and documents

Two carbon homologation of carboxylic acids using acrylamide as a radical trap

Barton, Derek H.R.,Liu, Wansheng

, p. 2431 - 2434 (2007/10/03)

Photolysis of O-acyl derivatives of N-hydroxy-2-thiopyridone in the presence of acrylamide in dichloromethane furnished crystalline 2-(pyridine-2-thiyl)-carboxamides. Desulfurization of the latter by nickel boride afforded primary amides in excellent yields.

The invention of radical reactions. Part XXXVIII. Homologation of carboxylic acids with acrylamide and synthetic studies of 3-deoxy-D-arabino-2-heptulosonic acid (DAH) and its 4-epimer

Barton, Derek H. R.,Liu, Wansheng

, p. 12067 - 12088 (2007/10/03)

Alkyl radicals generated from O-acyl derivatives of N-hydroxy-2-thiopyridone added onto acrylamide at room temperature to form crystalline 2-(2-pyridylsulfanyl)-carbosamides. Desulfurization of the latter by nickel boride at roam temperature afforded primary amides in quantitative yield. 3-Deoxy-D-arabino-2-heptulosonic acid (DAH), its 4-epimer, and their derivatives were effectively synthesized from commercial D-ribonolactone by similar radical chemistry.

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