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CAS

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198694-14-3

(E)-2-Phenyl-ethenesulfonic acid benzyl-(3-hydroxy-propyl)-amide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 198694-14-3 Structure

  • Basic information

    1. Product Name: (E)-2-Phenyl-ethenesulfonic acid benzyl-(3-hydroxy-propyl)-amide
    2. Synonyms: (E)-2-Phenyl-ethenesulfonic acid benzyl-(3-hydroxy-propyl)-amide
    3. CAS NO:198694-14-3
    4. Molecular Formula:
    5. Molecular Weight: 331.436
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 198694-14-3.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: (E)-2-Phenyl-ethenesulfonic acid benzyl-(3-hydroxy-propyl)-amide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-2-Phenyl-ethenesulfonic acid benzyl-(3-hydroxy-propyl)-amide(198694-14-3)
    11. EPA Substance Registry System: (E)-2-Phenyl-ethenesulfonic acid benzyl-(3-hydroxy-propyl)-amide(198694-14-3)

  • 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: 198694-14-3(Hazardous Substances Data)

198694-14-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 198694-14-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,6,9 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 198694-14:
(8*1)+(7*9)+(6*8)+(5*6)+(4*9)+(3*4)+(2*1)+(1*4)=203
203 % 10 = 3
So 198694-14-3 is a valid CAS Registry Number.

198694-14-3Relevant articles and documents

Stereoselective synthesis of isoxazole and pyrazole annulated sultams via intramolecular 1,3-dipolar cycloaddition reactions

Chiacchio, Ugo,Corsaro, Antonino,Gumina, Giuseppe,Pistara, Venerando,Rescifina, Antonio,Alessi, Manlio,Piperno, Anna,Romeo, Giovanni,Romeo, Roberto

, p. 13855 - 13866 (1997)

Functionalized isothiazoloisoxazole-4,4-dioxide, pyrazoloisothiazole-1,1-dioxide, [1,2]thiazinoisoxazole-4,4-dioxide and benzo[1,2]thiazinoisoxazole-4,4-dioxide systems have been obtained by intramolecular 1,3-dipolar cycloaddition, starting from substituted α- and β-sulfonamides.

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