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(E)-4-(4-{[(5-methyl-3-isoxazolyl)amino]sulfonyl}anilino)-4-oxo-2-butenoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 314282-26-3 Structure
  • Basic information

    1. Product Name: (E)-4-(4-{[(5-methyl-3-isoxazolyl)amino]sulfonyl}anilino)-4-oxo-2-butenoic acid
    2. Synonyms: (E)-4-(4-{[(5-methyl-3-isoxazolyl)amino]sulfonyl}anilino)-4-oxo-2-butenoic acid;(2E)-4-({4-[(5-methyl-1,2-oxazol-3-yl)sulfamoyl]phenyl}amino)-4-oxobut-2-enoic acid
    3. CAS NO:314282-26-3
    4. Molecular Formula: C14H13N3O6S
    5. Molecular Weight: 351.33
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 314282-26-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (E)-4-(4-{[(5-methyl-3-isoxazolyl)amino]sulfonyl}anilino)-4-oxo-2-butenoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-4-(4-{[(5-methyl-3-isoxazolyl)amino]sulfonyl}anilino)-4-oxo-2-butenoic acid(314282-26-3)
    11. EPA Substance Registry System: (E)-4-(4-{[(5-methyl-3-isoxazolyl)amino]sulfonyl}anilino)-4-oxo-2-butenoic acid(314282-26-3)
  • 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: 314282-26-3(Hazardous Substances Data)

314282-26-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 314282-26-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,4,2,8 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 314282-26:
(8*3)+(7*1)+(6*4)+(5*2)+(4*8)+(3*2)+(2*2)+(1*6)=113
113 % 10 = 3
So 314282-26-3 is a valid CAS Registry Number.

314282-26-3Downstream Products

314282-26-3Relevant articles and documents

Synthesis and characterization of novel sulfonamide functionalized maleimide polymers: Conventional kinetic analysis, antimicrobial activity and dielectric properties

Erol, Ibrahim

, (2022/02/03)

In this study, novel maleimide monomers, N-sulfamethoxazole maleimide(SMM), and N-sulfanilamide maleimide(SAM) were synthesized. Homopolymers of SMM and SAM were obtained by free radical polymerization method in 1,4-dioxane solvent at 65 °C. The structural characterizations of monomers and their homopolymers were carried out via FTIR, 1H- and 13C-NMR techniques. The glass transition temperature (Tg) of the polymers was determined using differential scanning calorimetry (DSC). Using the thermogravimetric analysis (TGA) method determined the thermal stability of the polymers. The thermal degradation activation energies (Ea) of the polymers were calculated by Kissinger, Flynn Wall Ozawa (FWO), and Kissinger-Akahira-Sunose (KAS) methods. The biological activities of compounds have been also studied on various bacteria and fungi. The weight average (Mw) and number average (Mn) molecular weights of the polymers were determined by gel permeation chromatography (GPC). Photochemical properties of polymers were investigated with ultraviolet (UV) and fourier transform infrared (FTIR) spectra. In addition, some physical constants of polymers such as density, solubility parameter, and viscosity were determined. Finally, the dielectric constant, dielectric loss factor and ac conductivity values ??of the polymers were estimated in the frequency range of 100 Hz–20 kHz.

Synthesis and studying the thermal properties of new maleimide polymers from sulfamethoxazole

Radhi, Ahmed Wheed,Zimam, Ezzat H.

, p. 4767 - 4771 (2021/08/31)

In this paper synthesis maleimide polymers from sulfamethoxazole via free radical polymerization method. The chemical structures of the prepared monomers and polymers confirmed by some spectroscopic analysis (FTIR, and NMR spectroscopies) besides the ther

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