52205-85-3

Usage

Uses

Used in Organic Chemistry:
INDANE-5-SULFONYL CHLORIDE is used as a reactive intermediate for the synthesis of complex organic molecules. Its reactivity allows chemists to create a variety of compounds with diverse applications in different industries.
Used in Pharmaceutical Industry:
INDANE-5-SULFONYL CHLORIDE is used as a building block in the development of new pharmaceutical compounds. Its ability to participate in various chemical reactions enables the creation of potential drug candidates with therapeutic properties.
Used in Material Science:
INDANE-5-SULFONYL CHLORIDE is used as a precursor in the synthesis of advanced materials, such as polymers and composites, which can be utilized in various applications, including electronics, automotive, and aerospace industries.
Used in Research and Development:
INDANE-5-SULFONYL CHLORIDE is used as a research tool in academic and industrial laboratories. Its reactivity and ability to form new compounds make it a valuable asset in the exploration of new chemical reactions and the discovery of novel compounds with potential applications.

InChI:InChI=1/C9H9ClO2S/c10-13(11,12)9-5-4-7-2-1-3-8(7)6-9/h4-6H,1-3H2

Upstream product

• 496-11-7 INDANE 
• 7790-94-5 chlorosulfonic acid 

Downstream Products

• 55119-14-7 indane-5-thiol 
• 35203-93-1 2,3-dihydro-5-indenylsulfonamide 
• 185098-53-7 1-(Indane-5-sulfonyl)-2-methoxy-4-phenyl-4,5-dihydro-1H-imidazole 
• 185098-63-9 1-(Indane-5-sulfonyl)-2-methoxy-5-phenyl-4,5-dihydro-1H-imidazole 
• 185098-61-7 1-(Indane-5-sulfonyl)-2-methoxy-4-p-tolyl-4,5-dihydro-1H-imidazole 
• 185098-71-9 1-(Indane-5-sulfonyl)-2-methoxy-5-p-tolyl-4,5-dihydro-1H-imidazole 
• 185098-57-1 4-(4-Chloro-phenyl)-1-(indane-5-sulfonyl)-2-methoxy-4,5-dihydro-1H-imidazole 
• 185098-67-3 5-(4-Chloro-phenyl)-1-(indane-5-sulfonyl)-2-methoxy-4,5-dihydro-1H-imidazole 
• 185098-56-0 4-(4-Bromo-phenyl)-1-(indane-5-sulfonyl)-2-methoxy-4,5-dihydro-1H-imidazole 
• 185098-66-2 5-(4-Bromo-phenyl)-1-(indane-5-sulfonyl)-2-methoxy-4,5-dihydro-1H-imidazole 
• 56096-73-2 2-(5-Indanylthio)benzoesaeure 
• 56096-77-6 2-(5-Indanylthio)phenylessigsaeure 
• 56096-76-5 2(5-Indanylthio)phenylacetonitril 
• 56096-75-4 2-(5-Indanylthio)benzylchlorid 

Relevant academic research and scientific papers

ANTITUMOR BENZOYLSULFONAMIDES

The present invention provides antitumor compounds of the formula (I); and antitumor methods.

Bispiperidines as antithrombotic agents

Novel compounds which are inhibitors of the binding of fibrinogen to the Gp IIb/IIIa platelet receptors, and which can be used therepeutically as antithrombotic agents

RADIKALIONEN 89. EINELEKTRONEN-OXIDATIONEN VON DIARYLDISULFIDEN MIT AlCl3/H2CCl2

The single electron oxidation of 14 alkyl and alkoxy substituted diaryldisulfides by AlCl3/H2CCl2 has been investigated by ESR/ENDOR spectroscopy.The radical cations observed prove the following skeletal rearrangements: Those with ring hydrogens in ortho positions to the disulfide bridge preferentially form thianthrene derivatives.The isomeric dinaphthyl disulfides react differently, the 2,2'-isomer yielding the dibenzothianthrene radical cation and the 1,1'-isomer the well-known naphthalene-1,8-disulfide radical cation.For all diaryl disulfides with completely alkyl- or methoxy-blocked ortho positions, oxidative desulfuration is observed.As substantiated by additional (2)D and (33)S isotope marking, the bis(2,5-dimethoxyphenyl)disulfide reacts both to the corresponding thianthrene derivative as well as via desulfuration to the radical cation of the monosulfide.Accompanying cyclovoltammetric and photoelectron spectroscopic measurements prove that all ESR spectroscopically detected radical cations result from compounds Ar-S-Ar, Ar-SS-Ar and Ar(S)2Ar with rather low oxidation or ionisation potentials and thus suggest that each the most easily oxidized paramagnetic species is observed in the rather complex product mixtures, which form on AlCl3/H2CCl2 oxidation of diaryldisulfides. Key words: Diaryl disulfides; one-electron oxidation; radical cations; ESR/ENDOR spectra.