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4-amino-2-chloro-5-(hydrazinocarbonyl)benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19806-88-3

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19806-88-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19806-88-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,0 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19806-88:
(7*1)+(6*9)+(5*8)+(4*0)+(3*6)+(2*8)+(1*8)=143
143 % 10 = 3
So 19806-88-3 is a valid CAS Registry Number.

19806-88-3Downstream Products

19806-88-3Relevant academic research and scientific papers

Synthesis of novel sulfonamides as potential antibacterial, antifungal and antimalarial agents

Mistry,Desai,Intwala

, p. 128 - 134 (2015/01/30)

4-Amino-2-chloro-5-(hydrazinocarbonyl)benzenesulfonamide 3 has been used as a precursor to synthesize some important biologically active heterocycles; which have been cyclized by treating with various aromatic acids in presence of POCl3 to give 4-amino-2-chloro-5-(5-substitutedphenyl-1, 3, 4-oxadiazol-2-yl) benzene sulfonamide 4a-j. Reaction of 4-amino-2-chloro-5-(hydrazinocarbonyl)benzenesulfonamide 3 with carbon disulphide in ethanol and potassium hydroxide yields the 1,3,4-oxadiazol derivatives 4. Condensation of this oxadiazole derivatives with different aromatic amines yields 4-amino-2-chloro-5-(5-mercapto-4-phenyl-4H-1,2,4-triazol-3-yl) benzene sulfonamide 5a-j and reaction of 4-amino-2-chloro-5-(hydrazinocarbonyl)benzenesulfonamide 3 with chloroacetamide in 2-ethoxy ethanol yields 1,2,4-triazine derivatives 6 which upon condensation with different aromatic aldehydes in presence of sodium methoxide yields 4-amino-5-[(6Z)-6-substitutedbenzylidene-5-oxo-1,2,5,6-tetrahydro-1,2,4-triazin-3-yl]-2-chlorobenzene sulfonamide 6a-j. The results indicate that some of the compounds show potential antibacterial, antifungal and antimalarial activity and comparable to those of commercial antibiotics and antimalarial compounds. The structures of novel synthesized compounds have been established on the basis of elemental analysis, IR, 1H NMR, 13C NMR and mass spectral data.

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