1603-40-3 | 3-Methylpyridin-2-amine

Packsize	Purity	Availability	Price	Discounted Price
25g	96%	in stock	$13.00	$9.00
100g	96%	in stock	$40.00	$28.00

Description

• Catalog Number: AB61002
• Chemical Name: 3-Methylpyridin-2-amine
• CAS Number: 1603-40-3
• Molecular Formula: C6H8N2
• Molecular Weight: 108.1411
• MDL Number: MFCD00006320
• SMILES: Cc1cccnc1N
• NSC Number: 450

Computed Properties

• Complexity: 72.9
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• XLogP3: 0.9

Upstream Synthesis Route

2-Amino-3-picoline, also known as 3-amino-2-picoline or 3-picolinylamine, is a valuable chemical intermediate commonly used in organic synthesis. Its versatile reactivity and unique molecular structure make it a crucial building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. In chemical synthesis, 2-Amino-3-picoline serves as a key component in the creation of heterocyclic compounds and complex organic molecules. It participates in various important reactions, including cyclizations, nucleophilic substitutions, and metal-catalyzed transformations. The presence of the amino group and the pyridine ring in 2-Amino-3-picoline provides it with significant functionality and allows for the modulation of properties such as solubility, reactivity, and biological activity in the final products. This compound is often employed in the synthesis of drug candidates, dyes, herbicides, and other fine chemicals due to its ability to impart desirable characteristics to the target molecules.Overall, 2-Amino-3-picoline plays a crucial role in chemical synthesis by enabling the construction of complex molecular structures with specific properties and functionalities, making it an indispensable tool for chemists working in various research and industrial settings.

Literature

• (Acetato-κ(2)O,O')(acetato-κO)bis(2-amino-3-methyl-pyridine-κN(1))cobalt(II).

  Acta crystallographica. Section E, Structure reports online 20121001

• Bis(2-amino-3-methyl-pyridine-κN(1))dichloridomercury(II).

  Acta crystallographica. Section E, Structure reports online 20120801

• Two hydration products of 3,4,5,6-tetrachloro-N-(methyl-2-pyridyl)phthalmic acids.

  Acta crystallographica. Section C, Crystal structure communications 20110701

• 2-Eth-oxy-6-[(3-methyl-pyridin-2-yl)-imino-meth-yl]phenol.

  Acta crystallographica. Section E, Structure reports online 20110501

• Synthesis and characterisation of two novel proton transfer compounds and their inhibition studies on carbonic anhydrase isoenzymes.

  Journal of enzyme inhibition and medicinal chemistry 20110201

• Synthesis, crystal structure, quantum chemical calculations, DNA interactions, and antimicrobial activity of [Ag(2-amino-3-methylpyridine)(2)]NO(3) and [Ag(pyridine-2-carboxaldoxime)NO(3)].

  Inorganic chemistry 20101101

• Bis(2-amino-3-methyl-pyridine)-dichlorido-cobalt(II).

  Acta crystallographica. Section E, Structure reports online 20101001

• 2-Amino-3-methyl-pyridinium 2-amino-5-methyl-pyridinium sulfate monohydrate.

  Acta crystallographica. Section E, Structure reports online 20091201

• 2-Methyl-N-[(3-methyl-2-pyrid-yl)carbamothio-yl]benzamide.

  Acta crystallographica. Section E, Structure reports online 20080501

• Metal-organic cooperative catalysis in C-H and C-C bond activation and its concurrent recovery.

  Accounts of chemical research 20080201

• Combining nucleoside analogues to achieve recognition of oligopurine tracts by triplex-forming oligonucleotides at physiological pH.

  FEBS letters 20051205

• Chelation-assisted carbon-hydrogen and carbon-carbon bond activation by transition metal catalysts.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20020603