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CAS

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863582-11-0

N-(4-hydroxy-8-methyl-5,8-dihydro-naphthalen-1-yl)-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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  • 863582-11-0 Structure

  • Basic information

    1. Product Name: N-(4-hydroxy-8-methyl-5,8-dihydro-naphthalen-1-yl)-4-methyl-benzenesulfonamide
    2. Synonyms: N-(4-hydroxy-8-methyl-5,8-dihydro-naphthalen-1-yl)-4-methyl-benzenesulfonamide
    3. CAS NO:863582-11-0
    4. Molecular Formula:
    5. Molecular Weight: 329.42
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 863582-11-0.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-(4-hydroxy-8-methyl-5,8-dihydro-naphthalen-1-yl)-4-methyl-benzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4-hydroxy-8-methyl-5,8-dihydro-naphthalen-1-yl)-4-methyl-benzenesulfonamide(863582-11-0)
    11. EPA Substance Registry System: N-(4-hydroxy-8-methyl-5,8-dihydro-naphthalen-1-yl)-4-methyl-benzenesulfonamide(863582-11-0)

  • 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: 863582-11-0(Hazardous Substances Data)

863582-11-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 863582-11-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,5,8 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 863582-11:
(8*8)+(7*6)+(6*3)+(5*5)+(4*8)+(3*2)+(2*1)+(1*1)=190
190 % 10 = 0
So 863582-11-0 is a valid CAS Registry Number.

863582-11-0Relevant articles and documents

Synthesis of the western half of the lolicines and lolitrems

England, Dylan B.,Magolan, Jakob,Kerr, Michael A.

, p. 2209 - 2212 (2006)

The synthesis of the highly substituted indole portion of the complex tremorgenic natural products lolicine A and B is presented. The Diels-Alder reaction of a quinone monoimine enables the synthesis of an appropriately substituted indole. The key step in

Synthesis and cross-coupling reactions of substituted 5-triflyloxyindoles

England, Dylan B.,Kerr, Michael A.

, p. 6519 - 6522 (2007/10/03)

N-Arylsulfonyl quinone monoimines undergo smooth cycloadditions in a [4+2] sense to yield the expected cycloadducts. The crude cycloadducts, when subjected to a short series of simple transformations, produce synthetically useful quantities of 5-triflylox

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