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1198777-57-9

N-(3,5-difluoro-2-methoxybenzylidene)-4-methylbenzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1198777-57-9 Structure

  • Basic information

    1. Product Name: N-(3,5-difluoro-2-methoxybenzylidene)-4-methylbenzenesulfonamide
    2. Synonyms: N-(3,5-difluoro-2-methoxybenzylidene)-4-methylbenzenesulfonamide
    3. CAS NO:1198777-57-9
    4. Molecular Formula:
    5. Molecular Weight: 325.336
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1198777-57-9.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-(3,5-difluoro-2-methoxybenzylidene)-4-methylbenzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(3,5-difluoro-2-methoxybenzylidene)-4-methylbenzenesulfonamide(1198777-57-9)
    11. EPA Substance Registry System: N-(3,5-difluoro-2-methoxybenzylidene)-4-methylbenzenesulfonamide(1198777-57-9)

  • 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: 1198777-57-9(Hazardous Substances Data)

1198777-57-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1198777-57-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,7,7 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1198777-57:
(9*1)+(8*1)+(7*9)+(6*8)+(5*7)+(4*7)+(3*7)+(2*5)+(1*7)=229
229 % 10 = 9
So 1198777-57-9 is a valid CAS Registry Number.

1198777-57-9Relevant articles and documents

Total synthesis of pentabromo- and pentachloropseudilin, and synthetic analogues-allosteric inhibitors of myosin ATPase

Martin, Rene,Jaeger, Anne,Bohl, Markus,Richter, Sabine,Fedorov, Roman,Manstein, Dietmar J.,Gutzeit, Herwig O.,Knolker, Hans-Joachim

, p. 8042 - 8046 (2009)

Stopping myo: The total syntheses of the title compounds have been achieved using a highly efficient silver(I)- catalyzed cyclization of N-tosyl-homopropargylamines. The pseudilin derivatives represent a novel class of myosin inhibitors. A new allosteric

Silver(I)-catalyzed route to pyrroles: Synthesis of halogenated pseudilins as allosteric inhibitors for myosin atpase and x-ray crystal structures of the protein-inhibitor complexes

Martin, Rene,Risacher, Celia,Barthel, Andre,Jaeger, Anne,Schmidt, Arndt W.,Richter, Sabine,Boehl, Markus,Preller, Matthias,Chinthalapudi, Krishna,Manstein, Dietmar J.,Gutzeit, Herwig O.,Knoelker, Hans-Joachim

, p. 4487 - 4505 (2014/08/05)

The pentahalogenated 2-arylpyrrole-type alkaloids pentabromopseudilin and pentachloropseudilin represent a new class of isoform-specific allosteric inhibitors of myosin ATPase. Herein, we describe an application of the silver(I)-catalyzed cycloisomerizati

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