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5-nitropyridine-2-sulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 75903-49-0 Structure
  • Basic information

    1. Product Name: 5-nitropyridine-2-sulfonamide
    2. Synonyms: 5-nitropyridine-2-sulfonamide
    3. CAS NO:75903-49-0
    4. Molecular Formula:
    5. Molecular Weight: 203.178
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 75903-49-0.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: 5-nitropyridine-2-sulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-nitropyridine-2-sulfonamide(75903-49-0)
    11. EPA Substance Registry System: 5-nitropyridine-2-sulfonamide(75903-49-0)
  • 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: 75903-49-0(Hazardous Substances Data)

75903-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75903-49-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,9,0 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75903-49:
(7*7)+(6*5)+(5*9)+(4*0)+(3*3)+(2*4)+(1*9)=150
150 % 10 = 0
So 75903-49-0 is a valid CAS Registry Number.

75903-49-0Upstream product

75903-49-0Downstream Products

75903-49-0Relevant articles and documents

Studies on Anticoccidial Agents. 13. Synthesis and Anticoccidial Activity of Nitropyridine-2- and -3-sulfonamides and Derivatives

Morisawa, Yasuhiro,Kataoka, Mitsuru,Nagahori, Hitoshi,Sakamoto, Toshiaki,Kitano, Noritoshi,et al.

, p. 1376 - 1380 (1980)

Eight nitropyridinesulfonamides andd pyridinesulfonamide N-oxides as their bioisosteres were prepared and evaluated for anticoccidial activity.Of these compounds, 2-, 4- and 5-nitropyridine-3-sulfonamides and pyridine-2- and -3-sulfonamide N-oxides were found to be active against Eimeria tenella.Thus, the relative positions, ortho or meta, of the substituents in nitropyridine-3-sulfonamides and pyridinesulfonamide N-oxides are important for anticoccidial activity.N-Substituted analogues of 5-nitropyridine-3-sulfonamide were also prepared and optimal anticoccidial activity was attained with the sulfonamide and its lower N-alkyl derivatives.The mode of action of 5-nitropyridine-3-sulfonamide was examined and found to be active in the sporozoite and the first schizogony stages.

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