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330824-97-0

N-(1-hexyl-buta-2,3-dienyl)-4-methyl-benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 330824-97-0 Structure

  • Basic information

    1. Product Name: N-(1-hexyl-buta-2,3-dienyl)-4-methyl-benzenesulfonamide
    2. Synonyms: N-(1-hexyl-buta-2,3-dienyl)-4-methyl-benzenesulfonamide
    3. CAS NO:330824-97-0
    4. Molecular Formula:
    5. Molecular Weight: 307.457
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 330824-97-0.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-(1-hexyl-buta-2,3-dienyl)-4-methyl-benzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(1-hexyl-buta-2,3-dienyl)-4-methyl-benzenesulfonamide(330824-97-0)
    11. EPA Substance Registry System: N-(1-hexyl-buta-2,3-dienyl)-4-methyl-benzenesulfonamide(330824-97-0)

  • 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: 330824-97-0(Hazardous Substances Data)

330824-97-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 330824-97-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,0,8,2 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 330824-97:
(8*3)+(7*3)+(6*0)+(5*8)+(4*2)+(3*4)+(2*9)+(1*7)=130
130 % 10 = 0
So 330824-97-0 is a valid CAS Registry Number.

330824-97-0Downstream Products

330824-97-0Relevant articles and documents

Palladium(0)-catalyzed carbonylation-coupling-cyclization of allenic sulfonamides with aryl iodides and carbon monoxide

Kang, Suk-Ku,Kim, Kwang-Jin

, p. 511 - 514 (2001)

(Matrix presented) α-Allenic sulfonamides undergo carbonylation-coupling-endo-cyclization with aryl iodides in the presence of Pd(PPh3)4 (5 mol %), K2CO3, and CO (20 atm) to form 3-aroyl-2- or 3-pyrrolines. Alte

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