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Phenol, 2-[3-(4-pyridinyl)-1,2,4-triazolo[3,4-b][1,3,4]thiadiazol-6-yl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

478362-80-0

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478362-80-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 478362-80-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,8,3,6 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 478362-80:
(8*4)+(7*7)+(6*8)+(5*3)+(4*6)+(3*2)+(2*8)+(1*0)=190
190 % 10 = 0
So 478362-80-0 is a valid CAS Registry Number.

478362-80-0Downstream Products

478362-80-0Relevant academic research and scientific papers

Synthesis of some 1, 2, 4-triazole derivatives and investigation of their fungicidal activities

Singh, Ram Janam,Singh, Dharmendra Kumar

, p. 235 - 239 (2011/10/08)

The synthesis of a series of 3-pyridyl-6-aryl-s-triazolo (3. 4-b) (1, 3. 4) - thiadiazoles are described, synthesis of 3-pyndyl-6-aryl-s-triazolo (3. 4-b) (1, 3, 4) - thiadiazoles (3a-m) have been achieved by the condensation of potassium dithiocarbazinate (1) with hydrazine hydrate and water. was under reflux 8 hours to yield 4-amino-3-pyridyl-5-mercapto-s-triazole (2). followed bv treatment with aromatic acid The compounds (3a-m) were characterized by spectral and elemental analyses. All thirteen compounds have been assayed for their fungicidal activity against P. oryzae. B. cinerea, A. nigar, C. albicans and T. rubrum. Compounds containing aryl substituents at position six and the 1. 2, 4-triazole moiety at position one or two showed reasonable fungicidal activity.

Synthesis and biological activity of some triazolothiadiazoles

Singh, Ram J.,Singh, Dharmendra K.

experimental part, p. 105 - 108 (2010/09/04)

The synthesis of a series of novel 3-pyridyl-6-aryl-s-triazolo[3,4-b]-[1,3, 4]-thiadiazoles is described. Fourteen new compounds were synthesized and characterized by spectral and elemental analyses. Some compounds were screened for antibacterial activity against S. aureus, E. coli, B. subtilis and P. aeruginosa. Compounds containing aryl substituents at position 6 and the 1,2,4-triazole moiety at position 1 or 2 showed reasonable antibacterial activity.

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