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CAS

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881417-28-3

Benzenesulfonamide, N-[2-[1-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4-hydroxybutyl]phenyl]- 4-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 881417-28-3 Structure

  • Basic information

    1. Product Name: Benzenesulfonamide, N-[2-[1-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4-hydroxybutyl]phenyl]- 4-methyl-
    2. Synonyms:
    3. CAS NO:881417-28-3
    4. Molecular Formula: C25H24N2O5S
    5. Molecular Weight: 464.542
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 881417-28-3.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: Benzenesulfonamide, N-[2-[1-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4-hydroxybutyl]phenyl]- 4-methyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenesulfonamide, N-[2-[1-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4-hydroxybutyl]phenyl]- 4-methyl-(881417-28-3)
    11. EPA Substance Registry System: Benzenesulfonamide, N-[2-[1-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4-hydroxybutyl]phenyl]- 4-methyl-(881417-28-3)

  • 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: 881417-28-3(Hazardous Substances Data)

881417-28-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 881417-28-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,4,1 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 881417-28:
(8*8)+(7*8)+(6*1)+(5*4)+(4*1)+(3*7)+(2*2)+(1*8)=183
183 % 10 = 3
So 881417-28-3 is a valid CAS Registry Number.

881417-28-3Downstream Products

881417-28-3Relevant articles and documents

Efficient synthesis of functionalized benzazepine derivatives utilizing intramolecular mitsunobu reaction

Ohtani, Tadaaki,Kawano, Yoshikazu,Kitano, Kazuyoshi,Matsubara, Jun,Komatsu, Makoto,Uchida, Minoru,Tabusa, Fujio,Nagao, Yoshimitsu

, p. 481 - 502 (2007/10/03)

The 5-hydroxy-2,3,4,5-tetrahydro-1H-benzazepine derivative (2), which is a typical metabolite of mozavaptan (1) having the 2,3,4,5-tetrahydro-1H-benzazepine skeleton, was synthesized by utilizing the intramolecular Mitsunobu reaction of the corresponding

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