611240-68-7

Basic information

• Product Name: 8-chloro-2-(trifluoromethyl)imidazo[1,2-a]pyrazine
• Synonyms: 8-chloro-2-(trifluoromethyl)imidazo[1,2-a]pyrazine
• CAS NO: 611240-68-7
• Molecular Formula: C₇H₃ClF₃N₃
• Molecular Weight: 221.57
• Mol File: 611240-68-7.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• Density: 1.68±0.1 g/cm3(Predicted)
• PKA: -2.72±0.30(Predicted)
• CAS DataBase Reference: 8-chloro-2-(trifluoromethyl)imidazo[1,2-a]pyrazine(CAS DataBase Reference)
• NIST Chemistry Reference: 8-chloro-2-(trifluoromethyl)imidazo[1,2-a]pyrazine(611240-68-7)
• EPA Substance Registry System: 8-chloro-2-(trifluoromethyl)imidazo[1,2-a]pyrazine(611240-68-7)

Safety Data

• Hazardous Substances Data: 611240-68-7(Hazardous Substances Data)

Usage

Description

8-chloro-2-(trifluoromethyl)imidazo[1,2-a]pyrazine is a heterocyclic organic compound with the molecular formula C7H3ClF3N3. It features a six-membered imidazo[1,2-a]pyrazine ring system, which is adorned with a chloro and trifluoromethyl functional group. 8-chloro-2-(trifluoromethyl)imidazo[1,2-a]pyrazine is recognized for its unique structure and properties, making it a valuable building block in the development of new molecules with potential therapeutic applications.

Uses

Used in Pharmaceutical Industry:
8-chloro-2-(trifluoromethyl)imidazo[1,2-a]pyrazine is utilized as a building block in the synthesis of various biologically active compounds. Its unique structure allows for the creation of new molecules with potential therapeutic applications, making it a valuable component in drug discovery and development.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, 8-chloro-2-(trifluoromethyl)imidazo[1,2-a]pyrazine serves as a key component in the synthesis of biologically active compounds. Its incorporation into agrochemical products can contribute to the development of effective solutions for pest control and crop protection.
Used in Drug Development:
8-chloro-2-(trifluoromethyl)imidazo[1,2-a]pyrazine is also studied for its potential as a drug candidate for the treatment of various diseases. Its unique chemical properties and structural features make it a promising candidate for further research and development into new therapeutic agents.

Upstream product

• 611240-67-6 8-chloro-2-(trifluoromethyl)-2,3-dihydroimidazo[1,2-a]pyrazin-2-ol hydrobromide 
• 107-12-0 propiononitrile 
• 6863-73-6 3-chloropyrazin-2-amine 
• 431-35-6 3-bromo-1,1,1-trifluoroacetone 
• 850445-47-5 8-hydroxy-2-(trifluoromethyl)imidazo[1,2-a]pyrazine 
• 777851-75-9 8-chloro-2-(trifluoromethyl)-2,3-dihydroimidazo[1,2-a]pyrazin-2-ol 

Downstream Products

• 611240-71-2 8-(4-fluorophenyl)-2-(trifluoromethyl)imidazo[1,2-a]pyrazine 
• 611240-69-8 8-methyl-2-(trifluoromethyl)imidazo[1,2-a]pyrazine 

Relevant articles and documents

METHOD OF CONTROLLING HARMFUL ARTHROPOD USING HETEROCYCLIC COMPOUND

PROBLEM TO BE SOLVED: To provide a method of controlling harmful arthropods. SOLUTION: An effective amount of a compound represented by formula (I) or an N oxide thereof is applied to harmful arthropods, a habitat of harmful arthropods, plants or the soil, [where Q is a group represented by Q1, or a group represented by Q2; Z is O or the like; A2 is CR4a or the like; A3 is N or CR4b or the like; B1 is CR1 or the like; B2 is N or CR6b or the like; B3 is N or CR6c or the like; G1 is N or CR3a; G2 is N or CR3b; G3 is N or CR3c; G4 is N or CR3d; R1 is a C1-C6 chain hydrocarbon group substituted with one or more substituents selected from the group consisting of a cyano group and a halogen atom, or the like; R2 is a C1-C6 alkyl group or the like; R3a, R3b, R3c and R3d are the same or different to represent a C1-C6 chain hydrocarbon group or the like; R4a, R4b, R6b and R6c are the same or different to represent H or the like; n is 0, 1 or 2.] SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

HARMFUL ARTHROPOD CONTROLLING METHOD USING HETEROCYCLIC COMPOUND

PROBLEM TO BE SOLVED: To provide a harmful arthropod controlling method. SOLUTION: Harmful arthropods can be controlled by a compound represented by formula (I): Q-Pyridyl (RS(O) substituted) [where Q is a group represented by the formula Q1 or a group re

Discovery of a potent, selective, and orally active phosphodiesterase 10A inhibitor for the potential treatment of schizophrenia

We report the discovery of a series of imidazo[1,2-a]pyrazine derivatives as novel inhibitors of phosphodiesterase 10A (PDE10A). In a high-throughput screening campaign we identified the imidazopyrazine derivative 1, a PDE10A inhibitor with limited select