38875-76-2

Usage

Uses

Used in Pharmaceutical Synthesis:
4-Chloro-6-methylnicotinonitrile is employed as a key intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs due to its unique chemical structure and properties.
Used in Agrochemical Production:
4-CHLORO-6-METHYLNICOTINONITRILE is also utilized in the production of agrochemicals, playing a crucial role in the creation of pesticides and other agricultural chemicals to enhance crop protection and yield.
Used in Organic Compounds Production:
4-Chloro-6-methylnicotinonitrile serves as a building block in the synthesis of other organic compounds, expanding its applications across various chemical industries.
Used in Research Applications:
Due to its unique characteristics, 4-Chloro-6-methylnicotinonitrile is commonly used in research settings to explore its properties and potential uses in chemical reactions and compound development.

InChI:InChI=1/C7H5ClN2/c1-5-2-7(8)6(3-9)4-10-5/h2,4H,1H3

Upstream product

• 473255-51-5 4-chloro-6-methylnicotinamide 
• 67367-33-3 4-hydroxy-6-methylnicotinic acid 
• 1073160-08-3 4-hydroxy-6-methylnicotinamide 
• 1073160-08-3 6-methyl-4-oxo-1,4-dihydro-pyridine-3-carboxylic acid amide 

Relevant academic research and scientific papers

SELECTIVE INHIBITORS OF CLINICALLY IMPORTANT MUTANTS OF THE EGFR TYROSINE KINASE

The present invention provides compounds of Formula (I) or a subgeneric structure or species thereof, or a pharmaceutically acceptable salt, ester, solvate, and/or prodrug thereof, and methods and compositions for treating or ameliorating abnormal cell pr

PYRAZOLE COMPOUNDS AND THEIR USE AS T-TYPE CALCIUM CHANNEL BLOCKERS

The invention relates to compounds of formula (I) Formula (I) wherein X, Y, R1, R2, (R4)n, and (R5)m are as defined in the description, and to pharmaceutically acceptable salts of such compounds. These compounds are useful as calcium T-channel blockers.

NEW SUBSTITUTED BIPHENYL ANALOGUES AS DUAL INHIBITORS OF AROMATASE AND SULFATASE

Provided are new biphenyl derivatives of formula (Ia). These compounds act as aromatase and sulfatase inhibitors. They are particularly useful for treating pathological conditions or diseases in which aromatase and sulfatase are involved. Moreover, provided are processes for the preparation of these compounds and pharmaceutical compositions containing said products and their use for the preparation of a medicament, in particular for the treatment of diseases characterized by aromatase and sulfatase activity such as hormone-dependent cancers.

SULFONYL AMIDE DERIVATIVES FOR THE TREATMENT OF ABNORMAL CELL GROWTH

The present invention relates to a compound of the formula I wherein R1 to R6, A, B, n and m are as defined herein. Such novel sulfonyl amide derivatives are useful in the treatment of abnormal cell growth, such as cancer, in mammals. This invention also relates to a method of using such compounds in the treatment of abnormal cell growth in mammals, especially humans, and to pharmaceutical compositions containing such compounds.