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10185-55-4

4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 10185-55-4 Structure

  • Basic information

    1. Product Name: 4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenesulfonamide
    2. Synonyms: 4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenesulfonamide
    3. CAS NO:10185-55-4
    4. Molecular Formula:
    5. Molecular Weight: 239.255
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10185-55-4.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: 4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenesulfonamide(10185-55-4)
    11. EPA Substance Registry System: 4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenesulfonamide(10185-55-4)

  • 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: 10185-55-4(Hazardous Substances Data)

10185-55-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10185-55-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,8 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10185-55:
(7*1)+(6*0)+(5*1)+(4*8)+(3*5)+(2*5)+(1*5)=74
74 % 10 = 4
So 10185-55-4 is a valid CAS Registry Number.

10185-55-4Downstream Products

10185-55-4Relevant articles and documents

The first one-pot ambient-temperature synthesis of 1,2,4-oxadiazoles from amidoximes and carboxylic acid esters

Baykov, Sergey,Sharonova, Tatyana,Shetnev, Anton,Rozhkov, Sergey,Kalinin, Stanislav,Smirnov, Alexey V.

, p. 945 - 951 (2017)

The first one-pot room-temperature protocol for the synthesis of 3,5-disubstituted-1,2,4-oxadiazoles via the condensation between amidoximes and carboxylic acid esters in superbase medium MOH/DMSO is reported. A broad spectrum of alkyl, aryl and hetaryl amidoximes and esters was examined. This reaction route provides convenient access to 1,2,4-oxadiazoles, which is highly desirable because in the light of this privileged scaffold is recognized as an important core in the design of novel therapeutic agents and high-tech materials.

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