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4-amino-5-(5-methoxy-3-phenyl-1H-indol-2-yl)-2,4-dihydro-[1,2,4]triazole-3-thione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

336612-66-9

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336612-66-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 336612-66-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,6,6,1 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 336612-66:
(8*3)+(7*3)+(6*6)+(5*6)+(4*1)+(3*2)+(2*6)+(1*6)=139
139 % 10 = 9
So 336612-66-9 is a valid CAS Registry Number.

336612-66-9Downstream Products

336612-66-9Relevant academic research and scientific papers

Synthesis and biological activities of fused biheterocycles containing indole nucleus: Reactions of 3-(5′-substituted-3′-phenylindol-2′-yl)-4-amino-4, 5-dihydro-s-triazol-5-thiones

Patil,Biradar

, p. 929 - 935 (2007/10/03)

5-(5′-Substituted-3′-phenylindol-2′-yl)-2,3-dihydro-1,3, 4-oxadiazol-2-thiones la-d on reaction with hydrazine hydrate in ethanol give 3-(5′-substituted-3′-phenylindol-2′-yl)-4-amino-4, 5-dihydro-s-triazole-5-thiones 2a-d. These compounds on reaction with phenacyl bromide, chloroacetic acid, cyanogen bromide, carbon disulphide and various aromatic acids furnish 7H-6-phenyl-3-(5′-substituted-3′-phenylindol-2′-yl)-s- triazolo[3,4-b][1,3,4]thiadiazines 3a-d, 7H-3-(5′-substituted-3′phenylindol-2′-yl)-s-triazolo [3,4-b][1,3,4]thiadiazin-6(5H)-ones 4a-d, 6-amino-3-(5′-substituted-3′-phenylin-dol-2′-yl)-s- triazolo[3,4-b][1,3,4]thiadiazoles 5a-d, 3-(5′.substituted-3′-phenylindol-2′-yl)-s-triazolo[3,4-b] [1,3,4]thiadiazole-6(5H)thiones 6a-d and 6-substituted-3-(5′-substituted-3′-phenylindol-2′-yl)-s- triazolo[3,4-b][1,3,4] thiadiazoles 7a-t. The characterisation of synthesized compounds has been done on the basis of elemental analysis, IR, 1H NMR and mass spectral data. All the newly synthesized compounds have been screened for their antimicrobial, anthelminthic, anti-inflammatory and anti-catatonic activities.

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