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128596-13-4

N-ethyl-thiocinnamamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 128596-13-4 Structure

  • Basic information

    1. Product Name: N-ethyl-thiocinnamamide
    2. Synonyms: N-ethyl-thiocinnamamide
    3. CAS NO:128596-13-4
    4. Molecular Formula:
    5. Molecular Weight: 191.297
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 128596-13-4.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: N-ethyl-thiocinnamamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-ethyl-thiocinnamamide(128596-13-4)
    11. EPA Substance Registry System: N-ethyl-thiocinnamamide(128596-13-4)

  • 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: 128596-13-4(Hazardous Substances Data)

128596-13-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128596-13-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,5,9 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 128596-13:
(8*1)+(7*2)+(6*8)+(5*5)+(4*9)+(3*6)+(2*1)+(1*3)=154
154 % 10 = 4
So 128596-13-4 is a valid CAS Registry Number.

128596-13-4Relevant articles and documents

GENERATION AND CYCLOADDITIONS OF 2-(N-ACYLAMINO)-1-THIA-1,3-DIENES. STRUCTURAL INVESTIGATIONS USING NMR METHODS. PART I.

Barnish, Ian T.,Fishwick, Colin W. G.,Hill, David R.,Szantay, Csaba

, p. 6771 - 6790 (1989)

A method has been developed for the efficient generation of 2-(N-acylamino)-1-thia-1,3-dienes.These novel hetero-dienes, which are generated via acylation of the corresponding thioamides, undergo irreversible regio- and stereospecific Diels-Alder addition to the starting thioamides to yield 6-(N-acylamino)-3,4-dihydro-2H-thiopyrans.The regiochemistry, relative configurations and the major solution conformations of the thiopyrans 4a-c and 10 have been determined using NMR techniques.In addition, it has been found that these systems exhibit a number of unique physical and chemical properties.

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