56358-04-4

Usage

Uses

Used in Organic Synthesis:
Nonyl(phenyl)sulfane is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions.
Used in Pharmaceutical and Agrochemical Development:
Nonyl(phenyl)sulfane is used as a sulfur transfer agent in chemical reactions, particularly in the development of pharmaceuticals and agrochemicals, due to its mild and selective reactivity.
Used in Specialty Chemicals Production:
Nonyl(phenyl)sulfane is used as an important intermediate in the manufacturing of specialty chemicals and industrial materials.
Used in Surfactant Manufacturing:
Nonyl(phenyl)sulfane is used as a crucial component in the production of surfactants and other industrial products, contributing to the advancement of science and technology.

Upstream product

• 693-58-3 1-Bromononane 
• 108-98-5 thiophenol 
• 113138-70-8 C₈H₁₇CH(SC₆H₅)2 
• 17882-12-1 4-trimethylsilylbenzenethiol 
• 850186-10-6 1-(4-trimethylsilylphenyl)thiononane 
• 882-33-7 diphenyldisulfane 
• 930-69-8 sodium thiophenolate 

Downstream Products

• 121411-02-7 S-methyl O-(1-phenyl-2-phenylthiodecyl) dithiocarbonate 
• 103863-83-8 N,N-Dimethyl-2-(4-nonylmercapto-benzhydrylmercapto)-ethylamin 
• 62839-71-8 (E)-1-phenyl-1-decene 
• 1731-84-6 nonanoic acid methyl ester 

Relevant academic research and scientific papers

Odorless diphenyl diselenide and disulfide: Syntheses and applications

Bis[4-(trimethylsilyl)phenyl]diselenide (3) and bis[4-(trimethylsilyl) phenyl]disulfide (31) are found to be odorless equivalents of the commonly used diphenyl diselenide and diphenyl disulfide, respectively. The diselenide 3 is shown to be useful in the preparation of odorless selenium(II) chloride 26 and selenium(IV) trichloride 28 that follow similar reactivity patterns to their phenyl derivatives and can be stored refrigerated under dry conditions. The corresponding selenium(II) bromide had to be prepared fresh from 3 before use. It is also shown that the trimethylsilyl group in the sulfide products can be protodesilylated quantitatively using TFA. Georg Thieme Verlag Stuttgart.

Reduction of dithioacetals with SmI2 in benzene-HMPA

Partial reduction of dithioacetals to the corresponding sulfides was effected by samarium iodide in the presence of either t-BuOH or acetic acid in benzene-HMPA. An α-sulfenyl anion was shown to be involved.