23837-10-7

Basic information

• Product Name: Benzene, 1-[bis(phenylthio)methyl]-4-methoxy-
• CAS NO: 23837-10-7
• Molecular Formula: C20H18OS2
• Molecular Weight: 338.494
• Mol File: 23837-10-7.mol
• Article Data: 20

Chemical Properties

• CAS DataBase Reference: Benzene, 1-[bis(phenylthio)methyl]-4-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-[bis(phenylthio)methyl]-4-methoxy-(23837-10-7)
• EPA Substance Registry System: Benzene, 1-[bis(phenylthio)methyl]-4-methoxy-(23837-10-7)

Safety Data

• Hazardous Substances Data: 23837-10-7(Hazardous Substances Data)

Upstream product

• 100-53-8 phenylmethanethiol 
• 882-33-7 diphenyldisulfane 
• 1078739-24-8 4-(4-methoxyphenyl)-1-tosyl-1H-1,2,3-triazole 
• 123-11-5 4-methoxy-benzaldehyde 
• 108-98-5 thiophenol 
• 110-66-7 n-pentanethiol 
• 2403-58-9 4-methoxybenzaldehyde diethylacetal 
• 2186-92-7 p-Anisaldehyde dimethyl acetal 
• 5023-67-6 4-methoxybenzyl phenyl sulfide 
• 40891-01-8 4-(dimorpholinomethyl)-1-methoxybenzene 

Downstream Products

• 1316843-77-2 (3R,4R)-3-(4-benzyloxy-3-methoxybenzyl)-4-(4-methoxybenzyl)dihydrofuran-2(3H)-one 
• 1567359-97-0 1-(4-methoxyphenyl)-4-methyl-2-(triisopropylsiloxy)-1,3-pentadiene 
• 1567359-98-1 1-(4-methoxyphenyl)-4-methyl-2-(triisopropylsiloxy)-1,3-pentadiene 
• 94550-08-0 ((4-methoxyphenyl)methylenedisulfonyl)dibenzene 
• 13087-56-4 1-(hepta-1,6-dien-4-yl)-4-methoxybenzene 
• 5023-67-6 4-methoxybenzyl phenyl sulfide 
• 123-11-5 4-methoxy-benzaldehyde 
• 18648-74-3 2,2-diphenyl-1-(4-methoxyphenyl)ethylene 

Relevant articles and documents

Synthesis and pharmacological characterisation of arctigenin analogues as antagonists of AMPA and kainate receptors

(-)-Arctigenin and a series of new analogues have been synthesised and then tested for their potential as AMPA and kainate receptor antagonists of human homomeric GluA1 and GluK2 receptors expressed in HEK293 cells using a Ca2+ influx assay. In general, these compounds showed antagonist activity at both receptors with greater activity evident at AMPARs. Schild analysis indicates that a spirocyclic analogue 6c acts as a non-competitive antagonist. Molecular docking studies in which 6c was docked into the X-ray crystal structure of the GluA2 tetramer suggest that (-)-arctigenin and its analogues bind in the transmembrane domain in a similar manner to the known AMPA receptor non-competitive antagonists GYKI53655 and the antiepileptic drug perampanel. The arctigenin derivatives described herein may serve as novel leads for the development of drugs for the treatment of epilepsy. This journal is

Visible-Light Photoredox-Catalyzed Thioacetalization of Aldehydes Under Metal-Free and Solvent-Free Conditions

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Rhodium-catalyzed denitrogenative thioacetalization of N-sulfonyl-1,2,3-triazoles with disulfides: An entry to diverse transformation of terminal alkynes

An efficient and useful rhodium-catalyzed denitrogenative thioacetalization of N-sulfonyl-1,2,3-triazoles has been developed for the first time. The protocol uses readily available N-sulfonyl-1,2,3-triazoles and diaryl disulfides as the starting materials. The corresponding hydrolytic and reductive products with thioacetals were obtained in good to excellent yields, and the reactions were carried out easily under mild conditions with tolerance of some functional groups. Furthermore, the generated thioacetals could be transformed into some useful compounds. Therefore, the present method provides a novel and valuable strategy for the diverse transformation of alkynes.