42416-20-6

Basic information

• Product Name: 2-(pyridin-2-ylthio)ethanamine(SALTDATA: 2HCl)
• Synonyms: 2-(pyridin-2-ylthio)ethanamine(SALTDATA: 2HCl);2-(2-pyridylsulfanyl)ethanamine;2-(2-pyridylthio)ethanamine;2-(2-pyridylthio)ethylamine;2-pyridin-2-ylsulfanylethanamine;2-(2-pyridinylthio)ethanamine
• CAS NO: 42416-20-6
• Molecular Formula: C₇H₁₀N₂S
• Molecular Weight: 227.15458
• Mol File: 42416-20-6.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(pyridin-2-ylthio)ethanamine(SALTDATA: 2HCl)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(pyridin-2-ylthio)ethanamine(SALTDATA: 2HCl)(42416-20-6)
• EPA Substance Registry System: 2-(pyridin-2-ylthio)ethanamine(SALTDATA: 2HCl)(42416-20-6)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 42416-20-6(Hazardous Substances Data)

Usage

General Description

2-(pyridin-2-ylthio)ethanamine is an organic compound with the molecular formula C7H10N2S. In its salt form, it is referred to as 2-(pyridin-2-ylthio)ethanamine dihydrochloride (2HCl). 2-(pyridin-2-ylthio)ethanamine(SALTDATA: 2HCl) consists of a pyridine ring attached to an ethanamine chain, with a thiol group (sulfur-hydrogen) attached to the pyridine ring. 2-(pyridin-2-ylthio)ethanamine has potential applications in pharmaceuticals and organic synthesis, particularly in the development of drugs targeting central nervous system disorders and antiviral agents. The dihydrochloride salt form of this compound is often used in research and laboratory settings as well.

Upstream product

• 151-56-4 ethyleneimine 
• 2637-34-5 2-Sulfanylpyridine 
• 870-24-6 2-chloroethanamine hydrochloride 
• 107-09-5 2-bromoethylamine 
• 109-09-1 2-chloropyridine 
• 156-57-0 2-mercaptoethylamine hydrochloride 
• 109-04-6 2-bromo-pyridine 
• 155965-47-2 2-[2'-(pyridin-2''-sulfanyl)ethyl]-1H-isoindole-1,3(2H)-dione 
• 689-98-5 chloroethylamine 

Downstream Products

• 106669-45-8 N-Benzoyl-N'-[3-(1H-imidazol-4-yl)-propyl]-N''-[2-(pyridin-2-ylsulfanyl)-ethyl]-guanidine 
• 1257527-86-8 RRRQRRCcystCcystRGY 

Relevant articles and documents

Antibacterial and catecholase activities of Co(III) and Ni(II) Schiff base complexes

X-ray structural analyses of two newly synthesized Schiff base-complexes, [Co(L)3] (1) and [Ni(L)2] (2) [HL = 2-((E)-(2-pyridine-2-pyridin-2-ylthio)ethylimino)methyl)phenol], reveal the bidentate chelation behavior of the ligand HL w

Pyrazole Compound

The present invention provides a pyrazole compound represented by the formula (I): wherein ring A0 is a pyrazole ring optionally further having 1 or 2 substituents; Ra is a substituted carbamoyl group; and Rb is an optionally substituted acylamino group, or a salt thereof or a prodrug thereof, which is useful as an agent for the prophylaxis or treatment of GSK-3β related pathology or disease, and a GSK-3β inhibitor including same.

INDANE DERIVATES AS MUSCARINIC RECEPTOR AGONISTS

The present invention relates to compounds of Formula I: I which are agonists of the M-1 muscarinic receptor.