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CAS

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1394828-32-0

N-[2-(cyclopent-2-en-1-yl)-4-methylphenyl]-4-methylbenzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1394828-32-0 Structure

  • Basic information

    1. Product Name: N-[2-(cyclopent-2-en-1-yl)-4-methylphenyl]-4-methylbenzenesulfonamide
    2. Synonyms: N-[2-(cyclopent-2-en-1-yl)-4-methylphenyl]-4-methylbenzenesulfonamide
    3. CAS NO:1394828-32-0
    4. Molecular Formula:
    5. Molecular Weight: 327.447
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1394828-32-0.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-[2-(cyclopent-2-en-1-yl)-4-methylphenyl]-4-methylbenzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[2-(cyclopent-2-en-1-yl)-4-methylphenyl]-4-methylbenzenesulfonamide(1394828-32-0)
    11. EPA Substance Registry System: N-[2-(cyclopent-2-en-1-yl)-4-methylphenyl]-4-methylbenzenesulfonamide(1394828-32-0)

  • 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: 1394828-32-0(Hazardous Substances Data)

1394828-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1394828-32-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,4,8,2 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1394828-32:
(9*1)+(8*3)+(7*9)+(6*4)+(5*8)+(4*2)+(3*8)+(2*3)+(1*2)=200
200 % 10 = 0
So 1394828-32-0 is a valid CAS Registry Number.

1394828-32-0Downstream Products

1394828-32-0Relevant articles and documents

Reactions of N-and C-alkenylanilines: IX.* synthesis, oxidation, and nitration of some 7-methyl-1,3a,4,8b-tetrahydrocyclopenta[b]indoles

Skladchikov, D. A.,Abdrakhmanov, I. B.,Gataullina, R. R.,Suponitskii, K. Yu.

, p. 957 - 967,11 (2012)

Heating of 4-acyl-3-iodo-7-methyl-1,2,3,3a,4,8b-hexahydrocyclopenta[b] indoles in piperidine gave 4-acyl-7-methyl-1,3a,4,8b-tetrahydrocyclopenta[b] indoles which were oxidized with KMnO4 to obtain the corresponding 4-acyl-7-methyl-1,2,3,3a,4,8b-hexahydrocyclopenta[b]indole-1,2-diols. Oxidation of 4-acyl-7-methyl-1,3a,4,8b-tetrahydrocyclopenta[b]indoles at the olefinic double bond with hydrogen peroxide in acetonitrile in the presence of formic acid afforded stereoisomeric epoxides with cis and trans orientation of the nitrogen-containing and oxirane rings. Nitration with a mixture of ammonium nitrate and trifluoroacetic anhydride produced 5-nitro derivatives. The structure of 1-{(1aR*,1bR*,6bS*,7aS*)-5-methyl-1a,1b,2, 6b,7,7ahexahydrooxireno[4,5]cyclopenta[1,2-b]indol-2-yl}ethanone was determined by X-ray analysis.

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