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CAS

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634616-27-6

Benzenesulfonamide, N-[[4-methoxy-3-(1-methylethoxy)-2-(1-propenyl)phenyl]methyl]-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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  • 634616-27-6 Structure

  • Basic information

    1. Product Name: Benzenesulfonamide, N-[[4-methoxy-3-(1-methylethoxy)-2-(1-propenyl)phenyl]methyl]-4-methyl -
    2. Synonyms:
    3. CAS NO:634616-27-6
    4. Molecular Formula: C21H27NO4S
    5. Molecular Weight: 389.516
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 634616-27-6.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-[[4-methoxy-3-(1-methylethoxy)-2-(1-propenyl)phenyl]methyl]-4-methyl -(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenesulfonamide, N-[[4-methoxy-3-(1-methylethoxy)-2-(1-propenyl)phenyl]methyl]-4-methyl -(634616-27-6)
    11. EPA Substance Registry System: Benzenesulfonamide, N-[[4-methoxy-3-(1-methylethoxy)-2-(1-propenyl)phenyl]methyl]-4-methyl -(634616-27-6)

  • 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: 634616-27-6(Hazardous Substances Data)

634616-27-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 634616-27-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,4,6,1 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 634616-27:
(8*6)+(7*3)+(6*4)+(5*6)+(4*1)+(3*6)+(2*2)+(1*7)=156
156 % 10 = 6
So 634616-27-6 is a valid CAS Registry Number.

634616-27-6Relevant articles and documents

Synthesis of substituted 2,3-dihydro-1H-2-benzazepines and 1,2-dihydroisoquinolines using an isomerization-ring-closing metathesis strategy: Scope and limitations

Panayides, Jenny-Lee,Pathak, Rakhi,De Koning, Charles B.,Van Otterlo, Willem A. L.

, p. 4953 - 4961 (2007)

An isomerization-ring-closing metathesis (RCM) approach was used for the synthesis of substituted 2,3-dihydro-1H-2-benzazepines and 1,2- dihydroisoquinolines. The 2,3-dihydro-1H-2-benzazepines were obtained from N-protected N-{2-[(1E)-prop-1-en-1-yl]benzy

Ruthenium-Mediated Isomerization and Ring-Closing Metathesis: Versatile Syntheses of 6-, 7- and 8-Membered Benzo-Fused Heterocycles

Van Otterlo, Willem A. L.,Pathak, Rakhi,De Koning, Charles B.

, p. 1859 - 1861 (2007/10/03)

Ruthenium-mediated isomerization and ring-closing metathesis (RCM) were the key steps used to convert a simple substrate, 2-allyl-3-isopropoxy-4-methoxybenzaldehyde, into a variety of 6-, 7- and 8-membered nitrogen- and oxygen-containing benzofused hetero

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