885276-99-3

Basic information

• Product Name: 2-AMINO-6-METHYL-PYRIDINE-3-CARBALDEHYDE
• Synonyms: 2-AMINO-6-METHYL-PYRIDINE-3-CARBALDEHYDE;2-AMINO-6-METHYLNICOTINALDEHYDE;3-Pyridinecarboxaldehyde, 2-amino-6-methyl-;2-aMino-6-Methyl-3-Pyridinecarboxaldehyde
• CAS NO: 885276-99-3
• Molecular Formula: C7H8N2O
• Molecular Weight: 136.15
• EINECS: 604-604-1
• Mol File: 885276-99-3.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 278.61 °C at 760 mmHg
• Flash Point: 122.299 °C
• Appearance: /
• Density: 1.206 g/cm³
• Vapor Pressure: 0.004mmHg at 25°C
• Refractive Index: 1.63
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: 2-AMINO-6-METHYL-PYRIDINE-3-CARBALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMINO-6-METHYL-PYRIDINE-3-CARBALDEHYDE(885276-99-3)
• EPA Substance Registry System: 2-AMINO-6-METHYL-PYRIDINE-3-CARBALDEHYDE(885276-99-3)

Safety Data

• Hazardous Substances Data: 885276-99-3(Hazardous Substances Data)

Usage

General Description

2-AMINO-6-METHYL-PYRIDINE-3-CARBALDEHYDE is a chemical compound with the molecular formula C8H8N2O. It is a derivative of pyridine, with a methyl group at the 6th position and an amino group at the 2nd position. The aldehyde group at the 3rd position makes it a reactive compound, suitable for use in organic synthesis. It can be used in the production of various pharmaceuticals, dyes, and other organic compounds. It is also used as a building block in the synthesis of heterocyclic compounds. Due to its complex structure and reactivity, 2-AMINO-6-METHYL-PYRIDINE-3-CARBALDEHYDE is of interest to synthetic chemists and researchers 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 articles and documents

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.

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