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94127-18-1

Benzenesulfonamide, 4-methyl-N-[9-[(4-methylphenyl)sulfonyl]-9H-carbazol-3-yl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Benzenesulfonamide, 4-methyl-N-[9-[(4-methylphenyl)sulfonyl]-9H-carbazol-3-yl]-

    Cas No: 94127-18-1

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  • 94127-18-1 Structure

  • Basic information

    1. Product Name: Benzenesulfonamide, 4-methyl-N-[9-[(4-methylphenyl)sulfonyl]-9H-carbazol-3-yl]-
    2. Synonyms:
    3. CAS NO:94127-18-1
    4. Molecular Formula: C26H22N2O4S2
    5. Molecular Weight: 490.604
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 94127-18-1.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, 4-methyl-N-[9-[(4-methylphenyl)sulfonyl]-9H-carbazol-3-yl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenesulfonamide, 4-methyl-N-[9-[(4-methylphenyl)sulfonyl]-9H-carbazol-3-yl]-(94127-18-1)
    11. EPA Substance Registry System: Benzenesulfonamide, 4-methyl-N-[9-[(4-methylphenyl)sulfonyl]-9H-carbazol-3-yl]-(94127-18-1)

  • 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: 94127-18-1(Hazardous Substances Data)

94127-18-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94127-18-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,1,2 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 94127-18:
(7*9)+(6*4)+(5*1)+(4*2)+(3*7)+(2*1)+(1*8)=131
131 % 10 = 1
So 94127-18-1 is a valid CAS Registry Number.

94127-18-1Relevant articles and documents

Palladium-Catalyzed Regioselective Synthesis of 1-Hydroxycarbazoles Under Aerobic Conditions

Youn, So Won,Kim, Young Ho,Jo, Yoon Hyung

, p. 462 - 468 (2019/01/04)

A palladium-catalyzed aerobic C?H amidation of N-Ts-2-amino-3′-hydroxylbiaryls has been developed to afford a diverse range of 1-hydroxycarbazoles with high regioselectivity and efficiency. This protocol benefits from operational simplicity, robustness, a

N-METHYL DERIVATIVES OF 3-AMINOCARBAZOLE

Kyziol, Janusz B.,Daszkiewicz, Zdzislaw

, p. 839 - 847 (2007/10/02)

Methylation of 3-aminocarbazole in presence of sodium hydrogencarbonate yields carbazolyl-3-trimethylammonium iodide, in alkaline media the fourth methyl group is introduced. 3-(N,N-Dimethylamino)-carbazoles were obtained from corresponding methiodides by lithium aluminium hydride reduction or by thermal decomposition.Synthesis of 3-(N-methylamino)-carbazole via tosylamide failed because of 3-(N-methyltosylamino)-9-tosylcarbazole cleaved only one sulfonamide bond.The method involving formylation of 3-aminocarbazole and reduction of the amide gave satisfactory results.

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