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1417156-24-1

N-allyl-1-(4-methoxycarbonylphenyl)-N-phenylmethanesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1417156-24-1 Structure

  • Basic information

    1. Product Name: N-allyl-1-(4-methoxycarbonylphenyl)-N-phenylmethanesulfonamide
    2. Synonyms: N-allyl-1-(4-methoxycarbonylphenyl)-N-phenylmethanesulfonamide
    3. CAS NO:1417156-24-1
    4. Molecular Formula:
    5. Molecular Weight: 345.419
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1417156-24-1.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: N-allyl-1-(4-methoxycarbonylphenyl)-N-phenylmethanesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-allyl-1-(4-methoxycarbonylphenyl)-N-phenylmethanesulfonamide(1417156-24-1)
    11. EPA Substance Registry System: N-allyl-1-(4-methoxycarbonylphenyl)-N-phenylmethanesulfonamide(1417156-24-1)

  • 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: 1417156-24-1(Hazardous Substances Data)

1417156-24-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1417156-24-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,7,1,5 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1417156-24:
(9*1)+(8*4)+(7*1)+(6*7)+(5*1)+(4*5)+(3*6)+(2*2)+(1*4)=141
141 % 10 = 1
So 1417156-24-1 is a valid CAS Registry Number.

1417156-24-1Relevant articles and documents

Access to a wide range of sultams by cyclodialkylation of α-substituted methanesulfonanilides

Rassadin, Valentin A.,Grosheva, Daria S.,Arefeva, Irina A.,Tomashevskiy, Aleksandr A.,Sokolov, Victor V.,De Meijere, Armin

, p. 5028 - 5037,10 (2020/08/24)

A wide range of five- and six-membered sultams bearing an α-ethoxycarbonyl-α-methyl substituent or an α-aryl group (17 examples) were synthesized by the cyclodialkylation of α-substituted methanesulfonanilides with α,ω-dihaloalkanes in the presence of K2CO3 or under phase-transfer catalysis (PTC) conditions. Upon treatment with K2CO3 in N,N-dimethylformamide (DMF) or NaH in dimethyl sulfoxide (DMSO), N-(2,3-dibromopropyl)-α- toluenesulfonanilides furnished different 1,3-diaryl-2-thia-3-azabicyclo[3.1.0] hexane 2,2-dioxides in good to excellent yields (51-88 %, 16 examples). The 4-methoxyphenyl (PMP) group was easily removed from the sultam nitrogen atom by treatment of the corresponding bicyclic sultams with cerium(IV) ammonium nitrate in acetonitrile (71-84 % yield, 6 examples). The intermolecular cyclodialkylation of α-substituted methanesulfonamides constitutes a simple and efficient route to five- and six-membered sultams with α-ethoxycarbonyl-α-methyl or α-aryl substitution. The intramolecular cyclodialkylation of N-(2,3-dibromopropyl)-α- toluenesulfanilides readily leads to bicyclic sultams bearing a cyclopropane ring. Copyright

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