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1,3,4-Thiadiazol-2-amine, 5-(2-chlorophenyl)-N-(phenylmethylene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84304-48-3

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84304-48-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84304-48-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,3,0 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 84304-48:
(7*8)+(6*4)+(5*3)+(4*0)+(3*4)+(2*4)+(1*8)=123
123 % 10 = 3
So 84304-48-3 is a valid CAS Registry Number.

84304-48-3Relevant academic research and scientific papers

Synthesis of thiadiazolo-s-triazines for their antiviral activity based on QSAR studies

Pandey,Tusi,Tandon,Joshi,Bajpai

, p. 2583 - 2588 (2007/10/03)

2-Amino-5-aralkyl-1,3,4-thiadiazole 1 on treatment with benzaldehyde yields 5-aralkyl-2-benzylideno-imino-1,3,4-thiadiazole 2 which on reaction with ammonium thiocyanate cyclises to give 2-phenyl-7-aralkyl-1,3,4-thiadiazolo-[3,2-a]-s-triazine-5-[6H,7H]-thione 3. Reaction of 3 with p-toluene sulphonyl chloride in anhydrous chloroform gives 2-phenyl-3-(p-toluenesulphonyl)-7-aralkyl-1,3,4-thiadiazolo-[3, 2-al-s-triazine-5-[6H,7H]-thiones 4g-I. Benzoyl chloride also reacts with 3 in anhydrous pyridine giving 2-phenyl-3-(benzoyl)-7-aralkyl-1,3,4-thiadiazolo-[3,2-a]-s-triazine-5-[6H,7H] -thiones 4a-f in quantitative yields. The antiviral activities of 4 based on QSAR studies have been reported using physicochemical method.

Studies on the synthesis and bioactivity of some thiadiazole derivatives

Padhy, Arun Kumar,Nag,Panda

, p. 998 - 1001 (2007/10/03)

Several 2-aryl-3-(4-aryl-1,3,4-thiadiazolyl)-4-thiazolidinones 3 and several other fused heterocycles 5 have been prepared. Most of the compounds 3 have been screened for their fungicidal activity against two fungi Aspergillus clavatus and Aspergillus fum

1,4-Cycloaddition of Isothiocyanates to Azomethines and Fungitoxicity of Resulting 1,3,4-Thiadiazolo-s-triazine-5(6H,7H)-thiones

Singh, H.,Yadav, L. D. S.,Sharma, K. S.

, p. 480 - 481 (2007/10/02)

Several 2,6,7-trisubstituted 1,3,4-thiadiazolo-s-triazine-5(6H,7H)-thiones have been prepared by 1,4-cycloaddition of aryl isothiocynates to 5-aryl(aryloxymethyl-2-benzylidene-amino-1,3,4-thiadiazoles (3a-e).The fungicidal activity of compounds has

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