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448196-03-0

4-tert-butyl-N-(2-methylphenyl)benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 448196-03-0 Structure

  • Basic information

    1. Product Name: 4-tert-butyl-N-(2-methylphenyl)benzenesulfonamide
    2. Synonyms: 4-tert-butyl-N-(2-methylphenyl)benzenesulfonamide
    3. CAS NO:448196-03-0
    4. Molecular Formula: C17H21NO2S
    5. Molecular Weight: 303.41914
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 448196-03-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-tert-butyl-N-(2-methylphenyl)benzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-tert-butyl-N-(2-methylphenyl)benzenesulfonamide(448196-03-0)
    11. EPA Substance Registry System: 4-tert-butyl-N-(2-methylphenyl)benzenesulfonamide(448196-03-0)

  • 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: 448196-03-0(Hazardous Substances Data)

448196-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 448196-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,8,1,9 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 448196-03:
(8*4)+(7*4)+(6*8)+(5*1)+(4*9)+(3*6)+(2*0)+(1*3)=170
170 % 10 = 0
So 448196-03-0 is a valid CAS Registry Number.

448196-03-0Downstream Products

448196-03-0Relevant articles and documents

Novel arylsulfoanilide-oxindole hybrid as an anticancer agent that inhibits translation initiation

Natarajan, Amarnath,Guo, Yuhong,Harbinski, Frederick,Fan, Yun-Hua,Chen, Han,Luus, Lia,Diercks, Jana,Aktas, Huseyin,Chorev, Michael,Halperin, Jose A.

, p. 4979 - 4982 (2007/10/03)

Structure-activity relationship studies of substituted arylsulfoanilides as antiproliferatives, which are mediated by the partial depletion of intracellular Ca2+ stores, resulted in the identification of compounds with micromolar activity against lung cancer cells in a growth inhibition assay. Incorporating the substitution pattern of the best arylsulfoanilides onto the 3-phenyloxindole scaffold resulted in a potent arylsulfoanilide-oxindole hybrid, 27. Compound 27 inhibits cancer cell growth by partial depletion of intracellular Ca2+ stores and phosphorylation of eIF2α.

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