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3-Propyl[1,2,4]triazolo[4,3-a]pyridine is a heterocyclic chemical compound with the molecular formula C8H10N4. It features a pyridine ring fused to a triazolopyridine ring, making it a versatile building block in organic synthesis and medicinal chemistry. 3-propyl[1,2,4]triazolo[4,3-a]pyridine has garnered interest due to its potential applications in various pharmaceutical and therapeutic areas.

4919-16-8

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4919-16-8 Usage

Uses

Used in Pharmaceutical Industry:
3-Propyl[1,2,4]triazolo[4,3-a]pyridine is used as a building block for the development of various pharmaceuticals. Its unique structure allows for the creation of diverse drug candidates with potential therapeutic properties.
Used in Organic Synthesis:
In the field of organic synthesis, 3-propyl[1,2,4]triazolo[4,3-a]pyridine serves as a key intermediate for the synthesis of complex organic molecules, contributing to the advancement of chemical research and the discovery of new compounds.
Used in Anticancer Research:
3-Propyl[1,2,4]triazolo[4,3-a]pyridine is used as a potential anti-cancer agent. It has been studied for its ability to target and inhibit the growth of cancer cells, making it a promising candidate for further research and development in oncology.
Used in Central Nervous System Modulation:
3-propyl[1,2,4]triazolo[4,3-a]pyridine has been investigated for its potential role as a modulator of the central nervous system. Its effects on neurological processes could lead to the development of treatments for various neurological disorders.
Used in Neurological Disorder Treatment:
3-Propyl[1,2,4]triazolo[4,3-a]pyridine is being explored for its potential use in the treatment of neurological disorders. Its interaction with the central nervous system may offer new avenues for managing and treating such conditions.
Used as a Drug Target:
In the realm of drug discovery, 3-propyl[1,2,4]triazolo[4,3-a]pyridine is considered a potential drug target for various diseases. Its unique chemical properties and biological activity make it a valuable point of interest for the development of targeted therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 4919-16-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,1 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4919-16:
(6*4)+(5*9)+(4*1)+(3*9)+(2*1)+(1*6)=108
108 % 10 = 8
So 4919-16-8 is a valid CAS Registry Number.

4919-16-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-propyl-[1,2,4]triazolo[4,3-a]pyridine

1.2 Other means of identification

Product number -
Other names 3-Propyl-s-triazolo<4,3-a>pyridin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4919-16-8 SDS

4919-16-8Downstream Products

4919-16-8Relevant academic research and scientific papers

Facile one pot synthesis of N-fused 1,2,4-triazoles via oxidative cyclisation using DDQ

Bhatt, Ashish,Singh, Rajesh K.,Kant, Ravi

, p. 236 - 247 (2018/11/23)

A facile and expedient one pot synthesis of N-fused 1,2,4-triazoles from 2-hydrazinopyridines or 2-hydrazinopyrazines and aldehydes is described via oxidative cyclization using DDQ as a safe and convenient oxidizing agent and polyethylene glycol as recyclable reaction medium. This protocol is effective toward various substrates having different functionalities. The easy recyclability of the reaction medium makes the process economic and potentially viable for commercial applications.

Synthesis of 1,2,4-Triazolo[4,3-a]pyridines and Related Heterocycles by Sequential Condensation and Iodine-Mediated Oxidative Cyclization

Li, Ertong,Hu, Zhiyuan,Song, Lina,Yu, Wenquan,Chang, Junbiao

, p. 11022 - 11027 (2016/07/27)

A facile and efficient approach to access 1,2,4-triazolo[4,3-a]pyridines and related heterocycles has been accomplished through condensation of readily available aryl hydrazines with corresponding aldehydes followed by iodine-mediated oxidative cyclizatio

A simple and efficient synthesis of 3,4,5-trisubstituted/N-fused 1,2,4-triazoles via ceric ammonium nitrate catalyzed oxidative cyclization of amidrazones with aldehydes using polyethylene glycol as a recyclable reaction medium

Nakka, Mangarao,Tadikonda, Ramu,Rayavarapu, Srinuvasarao,Sarakula, Prasanthi,Vidavalur, Siddaiah

, p. 517 - 525 (2015/02/19)

An environmentally benign protocol is described for the synthesis of 3,4,5-trisubstituted 1,2,4-triazoles and N-fused 1,2,4-triazoles via ceric ammonium nitrate catalyzed oxidative cyclization of amidrazones and aldehydes using polyethylene glycol as recyclable reaction medium. This protocol is effective toward various substrates having different functionalities. The easy recyclability of the reaction medium makes the process economic and potentially viable for commercial applications.

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