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3-(3-nitrophenyl)-[1,2,4]triazolo[4,3-a]pyridine is a complex organic chemical compound with the molecular formula C11H6N6O2. It features a triazolo[4,3-a]pyridine core, which is fused with a nitrophenyl group at the 3-position. 3-(3-nitrophenyl)-[1,2,4]triazolo[4,3-a]pyridine is characterized by its unique structure, which includes a triazole ring fused to a pyridine ring, and a nitro group attached to the phenyl ring. It is a yellow crystalline solid and is typically used in the synthesis of various pharmaceuticals and agrochemicals due to its potential biological activity. The compound's properties, such as its solubility and stability, can be influenced by the presence of the nitro group, making it a subject of interest in chemical research and development.

2746-38-5

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2746-38-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2746-38-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,4 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2746-38:
(6*2)+(5*7)+(4*4)+(3*6)+(2*3)+(1*8)=95
95 % 10 = 5
So 2746-38-5 is a valid CAS Registry Number.

2746-38-5Downstream Products

2746-38-5Relevant academic research and scientific papers

TBAI/TBHP-Catalyzed Synthesis of [1,2,4]Triazolo[4,3-a]pyridines and 3,5-Diaryl-1,2,4-oxadiazoles via Oxidative Cleavage of C=C Double Bond

Matcha, S. L.,Vidavalur, S.

, p. 1479 - 1486 (2021/10/26)

Abstract: A simple and efficient protocol has been described for the synthesis of [1,2,4]triazolo[4,3-a]pyri-dines and 3,5-disubstituted-1,2,4-oxadiazoles by reacting 2-hydrazinylpyridine and benzamidoximes, respec-tively, with styrenes via TBAI/TBHP-mediated oxidative cleavage of C=C bond under ligand- and metal-free conditions.

One-pot synthesis of N-fused 1,2,4-triazoles and related heterocycles via I2/TBHP-mediated oxidative C–N bond formation

Wu, Yachuang,Yang, Yifeng,Qi, Yinliang,Du, Shimei,Zhang, Yongsheng,Ding, Liang,Zhao, Yanfang

supporting information, p. 4216 - 4220 (2018/10/26)

A metal-free iodine/TBHP-mediated oxidative C–N bond formation for the one-pot synthesis of N-fused 1,2,4-triazoles and related heterocycles via cyclization has been developed. This reaction which is amenable to scale-up affords the corresponding products with good to excellent yields and tolerates a wide range of functional groups.

Efficient synthesis of 3-substituted 1,2,4-triazolo[4,3-a]pyridine by [bis(trifluroacetoxy)iodo]benzene-catalyzed oxidative intramolecular cyclization of heterocyclic hydrazones

Padalkar, Vikas S.,Patil, Vikas S.,Phatangare, Kiran R.,Umape, Prashant G.,Sekar

, p. 925 - 938 (2011/04/22)

A series of 1,2,4-triazolopyridines have been prepared by oxidative intramolecular cyclization of heterocyclic hydrazones with [bis(trifluroacetoxy) iodo]benzene. General applicability of this simple transformation was confirmed by synthesis of 1,2,4-triazolo[4,3-a]pyridine. The advantages of this protocol are the nontoxicity of catalyst and shorter reaction time to obtain good preparative yield.

A simple and efficient automatable one step synthesis of triazolopyridines from carboxylic acids

Wang, Ying,Sarris, Kathy,Sauer, Daryl R.,Djuric, Stevan W.

, p. 2237 - 2240 (2007/10/03)

Triazolopyridines can be rapidly and efficiently synthesized from a variety of carboxylic acids with 2-hydrazinopyridines in one simple step. The use of commercially available PS-PPh3 resin combined with microwave heating delivered the product

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