61686-65-5

Usage

Uses

Used in Pharmaceutical Industry:
PYRIDINE, 2,5-DIBROMO-3-(BROMOMETHYL)is used as a key building block in the synthesis of pharmaceuticals for its ability to contribute to the development of novel drug molecules. Its unique structure allows for the creation of a wide range of medicinal compounds with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, PYRIDINE, 2,5-DIBROMO-3-(BROMOMETHYL)serves as an essential component in the synthesis of various agrochemicals. Its incorporation aids in the production of effective pesticides, herbicides, and other agricultural chemicals that enhance crop protection and yield.
Used in Fine Chemicals Production:
PYRIDINE, 2,5-DIBROMO-3-(BROMOMETHYL)is utilized as a reagent in the preparation of fine chemicals, which are high-purity chemicals used in various industries, including fragrances, flavors, and specialty chemicals. Its role in these syntheses is crucial for achieving the desired chemical properties and purity levels.
Used in Chemical Intermediates Production:
PYRIDINE, 2,5-DIBROMO-3-(BROMOMETHYL)also plays a significant role as a reagent in the production of various chemical intermediates. These intermediates are essential precursors in the synthesis of a broad spectrum of chemical products, highlighting the versatility and importance of PYRIDINE, 2,5-DIBROMO-3-(BROMOMETHYL)in the chemical industry.

InChI:InChI=1/C6H4Br3N/c7-2-4-1-5(8)3-10-6(4)9/h1,3H,2H2

Upstream product

• 3430-18-0 2,5-dibromo-3-methylpyridine 
• 3430-21-5 5-bromo-3-methyl-pyridin-2-ylamine 

Downstream Products

• 1612855-02-3 C₅₀H₆₁N₉O₈S 
• 61686-64-4 1-benzyloxy-9,10-dihydro-2,9-diazaphenanthrene 
• 61686-67-7 1-benzyloxy-2,9-diazaphenanthrene 
• 7344-61-8 perlolidine 
• 61686-62-2 2-benzyloxy-5-dibromo-3-[(N-phenyl)aminomethyl]pyridine 
• 61686-66-6 2,5-dibromo-3-[(N-phenyl)aminomethyl]pyridine 

Relevant academic research and scientific papers

As hepatitis c inhibitor spiro compound and its use in medicine

The invention provides a spiro compound serving as a hepatitis c inhibitor and application thereof in a medicine. The compound is a compound as shown in a formula (I) or a stereisomer, a geometric isomer, a tautomer, nitric oxide, an aquo-complex, a solvate, a metabolite, pharmaceutically acceptable salt or prodrug of the compound as shown in the formula (I). The invention also provides a pharmaceutical composition containing the compound, application of the compound and the pharmaceutical composition in inhibition of HCV (Hepatitis C Virus) copy and HCV virus protein, as well as the application of the compound and the pharmaceutical composition in prevention, handling, treatment or relieving of HCV infection or hepatitis c disease for a patient. The formula I is as shown in the specification.

DIHYDROPYRROLOPYRIDINE INHIBITORS OF ROR-GAMMA

Provided are novel compounds of Formula (I): pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful in the treatment of diseases and disorders mediated by RORy. Also provided are pharmaceutical compositions co

Dihydropyrrolopyridine inhibitors of ROR-gamma

Provided are novel compounds of Formula (I): pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful in the treatment of diseases and disorders mediated by RORγ. Also provided are pharmaceutical compositions co

SPIRO RING COMPOUND AS HEPATITIS C VIRUS (HCV) INHIBITOR AND USES THEREOF FIELD OF THE INVENTION

A compound of formula (I) or a stereoisomer, a geometric isomer. a tautomer, an N-oxide, a hydrate, a solvate, a metabolite, a pharmaceutically acceptable salt or a prodrug thereof is provided, which can be used for treating HCV infection or a HCV disorder. Also a pharmaceutical composition comprising the compound and the use of the compound and the pharmaceutical composition thereof are provided, which can also be used for treating HCV infection or a HCV disorder.

Synthesis of the grass alkaloid perlolidine through a pyridyne cyclisation reaction

A synthesis of the grass alkaloid perlolidine is described in which the key step involves the pyridyne cyclisation of 2-benzyloxy-5-bromo-3-[(N-phenyl) aminomethyl] pyridine.