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3H-1,2,4-Triazole-3-thione, 2,4-dihydro-4-[[(2-nitrophenyl)methylene]amino]-5-(4-pyridinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

497231-69-3

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497231-69-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 497231-69-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,7,2,3 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 497231-69:
(8*4)+(7*9)+(6*7)+(5*2)+(4*3)+(3*1)+(2*6)+(1*9)=183
183 % 10 = 3
So 497231-69-3 is a valid CAS Registry Number.

497231-69-3Downstream Products

497231-69-3Relevant academic research and scientific papers

Synthesis of Schiff bases of 4-Amino-3-mercapto-5-pyridin-4yl-4H-1,2,4-triazole and their evaluation as SAR inducers

Majumder, Sujan,Bashyal, Bishnu Maya,Gupta

, p. 1260 - 1274 (2015/11/25)

A series of twenty five Schiff bases 6a-y of 4-Amino-3-mercapto-5-pyridin-4yl-4H-1,2,4-triazole having different substitution in the aryl ring attached to imine group designed incorporating the isonicotinic acid moiety present in INA, a known SAR inducer have been synthesized and characterized using 1H and 13C NMR, FT-IR spectroscopy and elemental analysis. All twenty five Schiff bases, 4-Arylideneamino-3-mercapto-5-pyridin-4-yl-4H-1,2,4-triazoles have been screened for systemic acquired resistance (SAR) inducing activity against sheath blight of rice and five potential compounds viz. 6f, 6g, 6r, 6t and 6u analogues have been further evaluated. All the five compounds have considerably decreased the relative lesion height (RLH) as compared to control with maximum reduction in RLH shown by compound 6u (47.15%). These five potential compounds have been further studied for their effect on phenol content, PAL and peroxidase activity. The compound 6u has been identified as the most potent SAR inducer both based on phenotypic and biochemical study and also does not show direct fungicidal activity against R. solani. Its RI activity is found better than 2,6-dichloroisonicotinic acid (INA), a resistance inducing chemical used as standard.

Efficient and convenient protocol for the synthesis of novel 1,2,4-triazolo[3,4-b][1,3,4]thiadiazines

Foroughifar, Naser,Mobinikhaledi, Akbar,Ebrahimi, Sattar

experimental part, p. 2421 - 2428 (2010/09/05)

The novel triazolothiadiazine analogs 5a-p were obtained via a multistep synthetic sequence beginning with 5-substituted 4-amino-1,2,4-triazole-3-thiols 1. Compound 1, in reaction with various aromatic aldehydes 2 in acetic acid, afforded Schiff bases 3a-

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