885276-99-3

Usage

Uses

Used in Pharmaceutical Industry:
2-AMINO-6-METHYL-PYRIDINE-3-CARBALDEHYDE is used as an intermediate in the synthesis of various pharmaceuticals for its ability to react and form new compounds with potential medicinal properties.
Used in Dye Industry:
In the dye industry, 2-AMINO-6-METHYL-PYRIDINE-3-CARBALDEHYDE is used as a chemical intermediate to produce dyes, capitalizing on its reactive aldehyde group to create diverse colorants.
Used in Organic Synthesis:
2-AMINO-6-METHYL-PYRIDINE-3-CARBALDEHYDE is used as a building block in organic synthesis for the creation of heterocyclic compounds, which are important in various chemical and pharmaceutical applications due to their unique properties and structures.
Used in Research and Development:
2-AMINO-6-METHYL-PYRIDINE-3-CARBALDEHYDE is utilized in research and development as a subject of study for synthetic chemists exploring new methods of synthesis and the compound's potential applications in various fields.

InChI:InChI=1/C7H8N2O/c1-5-2-3-6(4-10)7(8)9-5/h2-4H,1H3,(H2,8,9)

Upstream product

• 127446-32-6 2,2-Dimethyl-N-(3-formyl-6-methyl-2-pyridinyl)propanamide 
• 1824-81-3 2-Amino-6-methylpyridine 
• 86847-79-2 2,2-dimethyl-N-(6-methylpyridin-2-yl)propanamide 
• 84647-20-1 2-amino-6-methylpyridine-3-carbonitrile 

Relevant academic research and scientific papers

Photoinduced Trifluoromethylation of Arenes and Heteroarenes Catalyzed by High-Valent Nickel Complexes

We describe a series of air-stable NiIII complexes supported by a simple, robust naphthyridine-based ligand. Access to the high-valent oxidation state is enabled by the CF3 ligands on the nickel, while the naphthyridine exhibits either a monodentate or bidentate coordination mode that depends on the oxidation state and sterics, and enables facile aerobic oxidation of NiII to NiIII. These NiIII complexes act as efficient catalysts for photoinduced C(sp2)?H bond trifluoromethylation reactions of (hetero)arenes using versatile synthetic protocols. This blue LED light-mediated catalytic protocol proceeds via a radical pathway and demonstrates potential in the late-stage functionalization of drug analogs.

An enantioselective synthesis of (R)- and (S)-3-amino-7-methyl-3,4-dihydro- 1H-[1,8]naphthyridin-2-one

An enantioselective synthesis of (R)- and (S)-3-amino-7-methyl-3,4-dihydro- 1H-[1,8]naphthyridin-2-one via an asymmetric reduction and spontaneous cyclisation is reported.

HERBICIDAL COMPOUNDS

The present invention relates to novel herbicidal oxopyridine and thionopyridine derivatives of Formula (I), or an agronomically acceptable salt of said compound wherein R1, R5, R6, R7, X1, X2/s

HERBICIDAL COUMPOUNDS

The present invention relates to novel herbicidal [l,8]-naphthyridines of Formula (Ia) or (Ib), or an agronomically acceptable salt of said compound wherein R2, R3, R4, R5,R6,R7, R8, n, m, X and Q are as defined herein. The invention further relates to processes and intermediates for the preparation of the [l,8]-naphthyridines, to compositions which comprise the herbicidal compounds, and to their use for controlling weeds, in particular in crops of useful plants.