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Pyrazolo[1,5-a]pyridine-3-carbonitrile is a chemical compound characterized by the molecular formula C9H5N3. It is a pyridine derivative featuring a pyrazole ring fused to a pyridine ring, with a cyano group (-CN) at the 3-position. Pyrazolo[1,5-a]pyridine-3-carbonitrile is of interest to researchers in organic chemistry due to its potential applications in various fields, including pharmaceuticals, agrochemicals, material science, and organic electronics.

25627-89-8

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25627-89-8 Usage

Uses

Used in Pharmaceutical Industry:
Pyrazolo[1,5-a]pyridine-3-carbonitrile is used as a building block in the synthesis of various biologically active compounds. Its unique structure and functional groups make it a valuable component in the development of new pharmaceutical products with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, Pyrazolo[1,5-a]pyridine-3-carbonitrile serves as a key intermediate in the synthesis of agrochemicals, such as pesticides and herbicides. Its incorporation into these compounds can enhance their effectiveness in controlling pests and weeds, contributing to improved crop yields and agricultural productivity.
Used in Material Science:
Pyrazolo[1,5-a]pyridine-3-carbonitrile has potential applications in material science, where it can be utilized in the development of novel materials with specific properties. Its incorporation into materials may lead to advancements in areas such as polymers, coatings, and composites, offering new possibilities for various industrial applications.
Used in Organic Electronics:
In the field of organic electronics, Pyrazolo[1,5-a]pyridine-3-carbonitrile may find use in the design and fabrication of organic electronic devices, such as organic light-emitting diodes (OLEDs), organic solar cells, and organic field-effect transistors (OFETs). Its electronic properties and compatibility with other organic materials make it a promising candidate for enhancing the performance and functionality of these devices.
Overall, Pyrazolo[1,5-a]pyridine-3-carbonitrile is a versatile chemical compound with diverse potential applications across various industries. Its unique structure and properties make it an attractive candidate for further research and development, with the aim of unlocking its full potential in creating innovative products and solutions.

Check Digit Verification of cas no

The CAS Registry Mumber 25627-89-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,6,2 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 25627-89:
(7*2)+(6*5)+(5*6)+(4*2)+(3*7)+(2*8)+(1*9)=128
128 % 10 = 8
So 25627-89-8 is a valid CAS Registry Number.

25627-89-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name pyrazolo[1,5-a]pyridine-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 3-cyanopyrazolo<1,5-a>pyridine

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:25627-89-8 SDS

25627-89-8Relevant academic research and scientific papers

Synthesis of Functionalized Pyrazolo[1,5-a]pyridines: [3+2] Cycloaddition of N-Aminopyridines and α,β-Unsaturated Carbonyl Compounds/Alkenes at Room Temperature

Ravi, Chitrakar,Samanta, Supravat,Mohan, Darapaneni Chandra,Reddy, N. Naresh Kumar,Adimurthy, Subbarayappa

, p. 2513 - 2522 (2017/05/22)

The synthesis of functionalized pyrazolo[1,5-a]pyridines through oxidative [3+2] cycloaddition of N-aminopyridines with α,β-unsaturated carbonyl compounds or electron-withdrawing olefins is described. The reactions proceed in N-methylpyrrolidone as the solvent under metal-free conditions at room temperature.

MICROBIOCIDAL HETEROBICYCLIC DERIVATIVES

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Page/Page column 66; 67, (2017/04/08)

Compounds of the formula (I) wherein Q1, Q2, Y-X, R1, R2, R3, R4, Rb, Rc, Rd, R5, R6, R7, Ra, m and n are as defined in claim1. Furthermore, the present invention relates to agrochemical compositions which comprise compounds of formula (I), to preparation of these compositions, and to the use of the compounds or compositions in agriculture or horticulture for combating, preventing or controlling infestation of plants, harvested food crops, seeds or non-living materials by phytopathogenic microorganisms, in particular fungi.

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