15433-50-8

Upstream product

• 1122-41-4 2,4-dichlorobenzenethiol 
• 61713-34-6 2,4-dichloro-benzenethiol; sodium salt 
• 554-00-7 2,4-Dichloroaniline 
• 203051-52-9 N-(5'-Chloro-[1,1';3',1'']terphenyl-2'-yl)-S-(2,4-dichloro-phenyl)-thiohydroxylamine 
• 38064-02-7 2,4-dichlorobenzenesulfenyl chloride 

Downstream Products

• 4184-61-6 Monothiophosphorsaeure-O,O-dimethylester-S-<2,4-dichlor-phenylester> 
• 1452261-46-9 bis((2,4-dichlorophenyl)thio)methane 
• 1429474-39-4 3-((2,4-dichlorophenyl)thio)-6-methyl-1H-indole-2-carboxylic acid 
• 1369559-03-4 C₁₅H₉Cl₂NO₂S 
• 61713-35-7 2,4-Dichlorphenyl-methanthiosulphonat 
• 38064-02-7 2,4-dichlorobenzenesulfenyl chloride 

Relevant academic research and scientific papers

PIPERIDINE-DIONE DERIVATIVES FOR USE AS CONTRACEPTIVES

The invention relates to a method of reducing sperm motility or of contraception in a subject, said method comprising the step of administering to said subject an effective amount of a compound of formula (I), a stereoisomer, tautomer, pharmaceutically ac

LDHA ACTIVITY INHIBITORS

The invention provides compounds of formula (I), stereoisomers, tautomers, pharmaceutically acceptable salts and prodrugs thereof: (I) wherein A1 to A6 and R1 to R4 are as defined herein. Such compounds are suit

PYRIDOPYRROLIZINE AND PYRIDOINDOLIZINE DERIVATIVES

Pyridopyrrolizine and pyridoindolizine derivatives are prostaglandin receptor antagonists useful for the treatment of prostaglandin-mediated diseases such as allergic rhinitis, nasal congestion and asthma.

Stable Thioaminyl Radicals Having Functional Groups: Generation, ESR Spectra, Isolation, X-ray Crystallographic Analyses, and Magnetic Characterization of N-(Arylthio)-4-(ethoxycarbonyl)-2,6-diarylphenylaminyls, N-(Arylthio)-4-acetyl-2,6-diarylphenylaminyls, and N-(Arylthio)-4-cyano-2,6-diarylphenylaminyls

Oxidation of N-(arylthio)-4-(ethoxycarbonyl)-2,6-diarylanilines (9), N-(arylthio)-4-acetyl-2,6-diarylanilines (10), and N-(arylthio)-4-cyano-2,6-diarylanilines (11) with PbO2 yielded quite persistent N-(arylthio)-4-(ethoxycarbonyl)-2,6-diarylphenylaminyls(4), N-(arylthio)-4-acetyl-2,6-diarylphenylaminyls (5), and N-(arylthio)-4-cyano-2,6-diarylphenylaminyls (6), respectively, and they were isolated as pure radical crystals. On the other hand, N-(arylthio)-4-nitro-2,6-diarylphenylaminyls (6), and N-(arylthio)-4-chloro-2,6-diarylphenylaminyls (7), were unstable and soon decomposed. The X-ray crystallographic analyses of N-[(2,4-dichlorophenyl)thio]-4-acetyl-2,6-diphenylphenylaminyl (5c) and N-[(2,4-dichlorophenyl)thio]-4-cyano-2,6-diphenylphenylaminyl (6c) showed that the Ph-N-S-Ph π-framework is planar, and the 2- and 6-phenyl groups are twisted from the coplane. The ESR studies for 4-8 showed that their hyperfine coupling constants are nearly identical to each other and that the unpaired electron is extensively delocalized onto the anilino benzene ring and the arylthiyl group. The magnetic susceptibility measurements were carried out for five thioaminyl radical crystals and showed that one radical couples ferromagnetically with 2J/kB = 16.0 K, and the other four radicals couple antiferromagnetically with 2J/kB = -15.6 to -194.6 K or θ = -0.6 to -5.0 K.