463336-87-0

Usage

Uses

Used in Pharmaceutical Synthesis:
2-BROMO-6-ISOPROPOXYPYRIDINE is used as a building block in the synthesis of pharmaceuticals for its ability to contribute to the development of more complex molecular structures. Its unique reactivity and structural features make it a valuable component in the creation of new drugs.
Used in Agrochemical Synthesis:
In the agrochemical industry, 2-BROMO-6-ISOPROPOXYPYRIDINE is utilized as a key intermediate in the synthesis of various agrochemicals, playing a crucial role in the development of pesticides and other agricultural products to enhance crop protection and yield.
Used in Medicinal Chemistry Research:
2-BROMO-6-ISOPROPOXYPYRIDINE is employed as a research tool in medicinal chemistry, where its potential biological activities, such as antitumor and antiviral effects, are explored. Its unique structure allows researchers to investigate its interactions with biological targets and its potential use in therapeutic applications.
Used in Organic Synthesis:
As a compound with distinct reactivity, 2-BROMO-6-ISOPROPOXYPYRIDINE is used in organic synthesis for the preparation of a variety of organic compounds. Its bromine and isopropoxy substituents offer specific reaction pathways that can be harnessed in the synthesis of diverse organic molecules.
Used in Chemical Biology:
In the field of chemical biology, 2-BROMO-6-ISOPROPOXYPYRIDINE serves as a probe to study biological systems and interactions. Its unique structural elements allow it to be used in the investigation of molecular mechanisms and signaling pathways within biological organisms.

Upstream product

• 626-05-1 2,6-Dibromopyridine 
• 67-63-0 isopropyl alcohol 
• 27992-32-1 6-bromo-2-hydroxypyridine 
• 75-30-9 2-iodo-propane 

Relevant academic research and scientific papers

1,2-DIHYDRO-3H-PYRAZOLO[3,4-D]PYRIMIDIN-3-ONE DERIVATIVE AS WEE1 INHIBITOR

The present invention provides a 1,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one compound having an inhibitory effect on Wee 1, and includes an application of the compound in treating various types of tumors.

Phosphonic acid derivatives and application thereof

The invention belongs to the field of medical chemistry, relates to phosphonic acid derivatives for treating virus infectious diseases and an application thereof, and in particular, relates to the compounds represented by the formula (I) or isomers, pharmaceutically acceptable salts, solvates or prodrugs thereof, a preparation method thereof, pharmaceutical compositions containing the compounds and an application of the compounds or the compositions in preparation of drugs for treating the virus infection diseases.

BIARYL DERIVATIVE AS GPR120 AGONIST

The present invention relates to a biaryl derivative expressed by the chemical formula 1, a method for producing the biaryl derivative, a pharmaceutical composition comprising same, and use of same, the biaryl derivative expressed by the chemical formula 1, as a GPR120 agonist, promoting GLP-1 generation in the gastro-intestinal tract, reducing insulin resistance in the liver, muscles and the like from anti-inflammatory activity in the macrophage, pancreatic cells and the like, and allowing effective use in prevention or treatment of inflammation or metabolic diseases such as diabetes, complications from diabetes, obesity, non-alcoholic fatty liver disease, fatty liver disease, and osteoporosis.

LRRK2 INHIBITORS

Provided herein are compounds that inhibit or partially inhibit the activity of leucine rich repeat kinases. Also provided herein are methods of treatment of CNS disorders comprising administration of inhibitors of leucine rich repeat kinases.

AZOLE COMPOUNDS AS PIM INHIBITORS

The invention relates to bicyclic compounds of formulas I and Ia, and salts thereof. In some embodiments, the invention relates to inhibitors or modulators of Pim-1 and/or Pim-2, and/or Pim-3 protein kinase activity or enzyme function. In still further em

TRIAZOLE DERIVATIVES HAVING ANTIFUNGAL ACTIVITY, METHOD FOR THE PREPARATION THEREOF, AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME

A triazole derivative of formula 1 or a pharmaceutically acceptable salt, hydrate, solvate or isomer thereof is superior to the conventional antifungal drugs in antifungal activity against a wide spectrum of pathogenic fungi, and has advantageously low toxicity.

SPIROPIPERIDINE COMPOUNDS USEFUL AS BETA-SECRETASE INHIBITORS FOR THE TREATMENT OF ALZHERMER’S DISEASE

The present invention is directed to spiropiperidine compounds of formula (I) which are inhibitors of the beta-secretase enzyme and that are useful in the treatment of diseases in which the beta-secretase enzyme is involved, such as Alzheimer's disease. T

Heterocyclic compounds as inhibitors of factor VIIa

The present invention relates generally to compounds that inhibit serine proteases. In particular it is directed to novel heterocyclic compounds, or a stereoisomer or pharmaceutically acceptable salt, solvate, or prodrug form thereof, which are useful as selective inhibitors of serine protease enzymes of the coagulation cascade; for example thrombin, factor VIIa, factor Xa, factor XIa, factor IXa, and/or plasma kallikrein. In particular, it relates to compounds that are factor VIIa inhibitors. This invention also relates to pharmaceutical compositions comprising these compounds and methods of using the same.