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177972-59-7

N-[(3Z)-hex-3-en-1-yl](4-methylphenyl)sulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 177972-59-7 Structure

  • Basic information

    1. Product Name: N-[(3Z)-hex-3-en-1-yl](4-methylphenyl)sulfonamide
    2. Synonyms: N-[(3Z)-hex-3-en-1-yl](4-methylphenyl)sulfonamide
    3. CAS NO:177972-59-7
    4. Molecular Formula:
    5. Molecular Weight: 253.365
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 177972-59-7.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-[(3Z)-hex-3-en-1-yl](4-methylphenyl)sulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[(3Z)-hex-3-en-1-yl](4-methylphenyl)sulfonamide(177972-59-7)
    11. EPA Substance Registry System: N-[(3Z)-hex-3-en-1-yl](4-methylphenyl)sulfonamide(177972-59-7)

  • 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: 177972-59-7(Hazardous Substances Data)

177972-59-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 177972-59-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,9,7 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 177972-59:
(8*1)+(7*7)+(6*7)+(5*9)+(4*7)+(3*2)+(2*5)+(1*9)=197
197 % 10 = 7
So 177972-59-7 is a valid CAS Registry Number.

177972-59-7Relevant articles and documents

Synthesis of cyclic dienamide using ruthenium-catalyzed ring-closing metathesis of ene-ynamide

Mori, Miwako,Wakamatsu, Hideaki,Saito, Nozomi,Sato, Yukako,Narita, Rie,Sato, Yoshihiro,Fujita, Reiko

, p. 3872 - 3881 (2007/10/03)

Ring-closing metathesis of ene-ynamide, which has alkene and ynamide moieties in a molecule, using a second-generation ruthenium carbene complex produced nitrogen-containing heterocycles, which have a dienamide moiety, in high yields. Diels-Alder reaction

A new, simple synthesis of N-tosyl pyrrolidines and piperidines

Marcotullio, Maria Carla,Campagna, Valerio,Sternativo, Silvia,Costantino, Ferdinande,Curini, Massimo

, p. 2760 - 2766 (2008/02/05)

Iodocyclization of unsaturated tosylamides promoted by Oxone oxidation of KI afforded, in good yields, N-tosyl iodopyrrolidines and piperidines. A new, simple method for the conversion of alcohols to tosylamides is presented. Georg Thieme Verlag Stuttgart.

A stereochemically flexible approach to pyrrolidines based on 5-endo-trig iodocyclisations of homoallylic sulfonamides

Jones,Knight,Hibbs

, p. 1182 - 1203 (2007/10/03)

5-endo-trig Iodocyclisations of the (E)-homoallylic sulfonamides 24 in the presence of potassium carbonate give excellent yields of trans-2,5-disubstituted-3-iodopyrrolidines 36. In the absence of base, these initial kinetic products undergo rapid isomeri

A new, highly stereoselective approach to pyrrolidines via overall 5-endo-trig cyclisations of homoallylic tosylamides

Jones, Andrew D.,Knight, David W.

, p. 915 - 916 (2007/10/03)

Iodocyclisations of E-homoallylic tosylamides 7 lead to excellent yields of either 2,5-trans- or 2,5-cis-3-iodopyrrolidines (10 or 11), depending upon the reaction conditions.

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