3144-93-2

Usage

Appearance

Yellow crystalline solid

Odor

Strong and unpleasant

Function

Acts as a reagent for the synthesis of dithiolanes and related compounds

Reactions

Can undergo reactions with various functional groups, including carbonyl compounds and esters, to form dithiolanes

Versatility

Widely used in organic chemistry due to its ability to efficiently create sulfur-containing compounds

Applications

Pharmaceutical, agrochemical, and materials chemistry

Safety

Highly reactive and can pose health hazards if not used properly

Handling

Should be handled with caution

Upstream product

• 108-44-1 1-amino-3-methylbenzene 
• 130-15-4 [1,4]naphthoquinone 
• 83-72-7 2-hydroxynaphtho-1,4-quinone 
• 27699-96-3 4-(3-methylphenylamino)-1,2-naphthoquinone 
• 2348-81-4 2-amino-1,4-naphthoquinone 
• 17933-03-8 m-tolylboronic acid 

Relevant academic research and scientific papers

Photoinduced EDA Complexes Enabled Radical Tandem Cyclization/Arylation of Unactivated Alkene with 2-Amino-1,4-naphthoquinones

A visible-light-induced radical tandem cyclization/arylation between 2-amino-1, 4-naphthoquinone and N-allyl-2-bromo-2,2-difluoroacetamides has been developed without an external photocatalyst. The transformation could be carried out at room temperature a

Transition metal mediated selective C vs N arylation of 2-aminonaphthoquinone and its application toward the synthesis of benzocarbazoledione

Selective C vs N-arylation of 2-aminonaphthoquinone was achieved using different transition metal salts and arylboronic acids. Mn(OAc)3·2H2O provided C-arylated product whereas NiCl2·6H2O and Cu(OAc)2

Isomerization of 4-arylamino-1,2-naphthoquinones to 2-arylamino-1,4-naphthoquinones

4-Arylamino-1,2-naphthoquinones isomerize into 2-arylamino-1,4-naphthoquinones upon refluxing in acetic acid. The isomerization follows two routes via intermediate 2-hydroxy-1,4-naphthoquinone and 2-arylamino-1,4-naphthoquinone 4-N-arylimines.

Synthesis of novel substituted methoxybenzo[2,3-b]carbazole derivatives via C-H functionalization. Experimental and theoretical characterization of their photophysical properties

The novel, highly blue, fluorescent N-methyl-6,11-dimethoxybenzo[2,3-b]carbazole derivatives were prepared by oxidative coupling of anilines with naphthoquinone followed by palladium catalyzed oxidative [Formula presented] functionalization and a one pot

An experimental and theoretical study of the substituent effects on the redox properties of 2-[(R-phenyl)-amine]-1,4-naphthalenediones in acetonitrile

We synthesized and analyzed 19 compounds of 3'- (meta-) and 4'-(para-) substituted 2-[(R-phenyl)amine]-1,4-naphthalenediones (PANs) R = p-MeO, p- Me, p-Bu, p-Hex, p-Et, m-Me, m-Et, H, p-Cl, p-Br, m-F, m-Cl, p-COCH3, m-CN, m-NO2, m-CO