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150780-40-8

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150780-40-8 Usage

Description

IMIDAZO[1,2-A]PYRIDINE, 6-BROMO-2-(TRIFLUOROMETHYL)is a chemical compound that belongs to the imidazo[1,2-a]pyridine class. It is characterized by the presence of a bromine atom and a trifluoromethyl group, which are significant functional groups in organic chemistry. These features contribute to its unique structure and reactivity, making it a promising candidate for various applications in fields such as pharmaceuticals, agrochemicals, and material science. Its properties and potential uses highlight its value for chemical synthesis and research in organic chemistry.

Uses

Used in Pharmaceutical Industry:
IMIDAZO[1,2-A]PYRIDINE, 6-BROMO-2-(TRIFLUOROMETHYL)is used as a pharmaceutical intermediate for the development of new drugs. Its unique structure and reactivity allow for the design and synthesis of novel compounds with potential therapeutic effects. The bromine and trifluoromethyl groups can be further modified or used as starting points for the creation of bioactive molecules targeting specific diseases or conditions.
Used in Agrochemical Industry:
In the agrochemical industry, IMIDAZO[1,2-A]PYRIDINE, 6-BROMO-2-(TRIFLUOROMETHYL)is used as a building block for the synthesis of new agrochemicals. Its chemical properties can be exploited to create compounds with pesticidal, herbicidal, or fungicidal properties, contributing to the development of more effective and environmentally friendly agricultural products.
Used in Material Science:
IMIDAZO[1,2-A]PYRIDINE, 6-BROMO-2-(TRIFLUOROMETHYL)is utilized in material science for the development of new materials with specific properties. Its unique structure and reactivity can be employed to synthesize compounds with potential applications in areas such as polymers, dyes, or sensors. The bromine and trifluoromethyl groups can be tailored to achieve desired characteristics, such as improved stability, solubility, or conductivity.
Overall, the versatility of IMIDAZO[1,2-A]PYRIDINE, 6-BROMO-2-(TRIFLUOROMETHYL)in various industries is a testament to its potential as a valuable chemical compound for research and development. Its unique structure and reactivity make it an attractive target for chemical synthesis and exploration of new applications in diverse fields.

Check Digit Verification of cas no

The CAS Registry Mumber 150780-40-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,7,8 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 150780-40:
(8*1)+(7*5)+(6*0)+(5*7)+(4*8)+(3*0)+(2*4)+(1*0)=118
118 % 10 = 8
So 150780-40-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H4BrF3N2/c9-5-1-2-7-13-6(8(10,11)12)4-14(7)3-5/h1-4H

150780-40-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Bromo-2-trifluoromethylimidazo[1,2-a]pyridine

1.2 Other means of identification

Product number -
Other names 6-Bromo-2-(trifluoromethyl)imidazo[1,2-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:150780-40-8 SDS

150780-40-8Relevant articles and documents

Modification of biologically active amides and amines with fluorine-containing heterocycles 8. γ-Carbolines modified with the 2-(2-trifluoromethylimidazo[1,2-a]pyridin-6-yl)ethyl fragment

Sokolov,Aksinenko, A. Yu.,Grigoriev,Bachurin

, p. 199 - 202 (2013)

An approach to modification of biologically active g-carbolines with the 2-(2-trifluoromethylimidazo[1,2-a]pyridin-6-yl)ethyl fragment was proposed. The modification involves a reaction of 2-trifluoromethyl-6-vinylimidazo[1,2-a] pyridine with g-carbolines. The effect of the compounds obtained on neuronal NMDA receptors was studied by the radioligand binding method.

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