69981-39-1

Usage

Uses

Used in Organic Synthesis:
(2-(tosyloxy)ethyl)disulfide is used as a reagent for the formation of carbon-carbon and carbon-sulfur bonds. Its reactivity allows for the creation of various organic compounds, making it a valuable component in the synthesis process.
Used as a Precursor in Synthesis:
(2-(tosyloxy)ethyl)disulfide also serves as a precursor in the synthesis of various organic compounds. Its presence in the initial stages of a reaction can lead to the development of a wide range of products, showcasing its importance in the field of organic chemistry.

Upstream product

• 1892-29-1 bis(2-hydroxyethyl) disulfide 
• 98-59-9 p-toluenesulfonyl chloride 

Relevant academic research and scientific papers

Selective photosensitization through an and logic response: Optimization of the pH and glutathione response of activatable photosensitizers

A series of pH and GSH responsive photosensitizers were designed and synthesized. pKa values were optimized by adjusting the inductive contribution of substituents to reach a pH range (6.0-7.4) relevant to the tumour microenvironment. pH-Activatable behaviour and redox mediated release of the quencher from the PS by GSH allow the construction of an AND logic operator for selective photodynamic action in aqueous solutions.

Disulfide-bridge dimeric porphyrin and their reference compounds for glutathione-based specific tumor-Activation

The tumor micro-environment is rich in glutathione. To exploit this feature for tumor-Activatable porphyrin-based photosensitizers, a dimeric disulfide-bridged porphyrin has been designed and prepared, together with two reference derivatives, a non-cleava

PROGRAMMABLE THERMORESPONSIVE GELS

Provided herein, inter alia, are non-crosslinked polymers that possess thermoresponsive properties. These polymers possess a cleavable bond that breaks under certain conditions The disclosure also provides pharmaceutical compositions containing the polyme

Reduction-degradable linear cationic polymers as gene carriers prepared by Cu(I)-catalyzed azide-alkyne cycloaddition

Linear reduction-degradable cationic polymers with different secondary amine densities (S2 and S3) and their nonreducible counterparts (C2 and C3) were synthesized by Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) step-growth polymerization of the dia

STYRYL SULFIDE DYES

Disclosed are composition and method for dyeing keratin-containing fibers comprising or utilizing styryl sulfide dyes of formula (1), their salts, isomers, hydrates and other solvates, wherein R1, R′1, R2, R′2, R3, R′3, W1, W′1, W2, W′2, W3, W′3, W4, W′4, Q, Q′, Y1 and Y2 are defined in claims and disclosure.

PYRIDO-THIAZINIUM DYES

Disclosed is a method of dyeing keratin-containing fibers comprising treating the fiber with at least one compound of formula (1), wherein R1, R2, R3, R4 independently from each other are hydrogen; hydroxy; -S-H

SULFIDE DYES

Formula (I) wherein R1 and R2 each independently from each other are a residue of an organic dye; Y1 and Y2 each independently from each other are unsubstituted or substituted, straightchain or branched, interrupted or uninterrupted -C1-C10alkylene-; -C5-C10cycloalkylene-; C5-C10arylene; or-C5-C10arylene-(C1-C10alkylene)-; Z1 and Z2 independently from each other are Formula (II) are each independently from each other hydrogen; or unsubstituted or substituted, straight-chain or branched, monocyclic or polycyclic, interrupted or uninterrupted C1-C14alkyl; C2-C14alkenyl; C6-C10aryl; C6-C10aryl-C1-C10alkyl; or C5-C10alkyl(C5-C10aryl); r, q and n independently from each other are 0 or 1, if n is 0, Z3 is hydrogen; and if n is 1, Z3 is -S-; with the proviso that the method does not comprise treating the fiber with an enzyme of the type of a protein disulfidisomerase (EC 5.3.4.1). Further, the present invention relates to novel disulfid compounds, compositions thereof, especially comprising other dyes, and to processes for their preparation.

New oncostatic nitrosourea of clinical interest. II. Study of CNCC constituents

CNCC is an isomeric mixture of dinitrosated chloroethyl nitrosoureas. Two of these being identified, a complete analysis of the isolated mixture obtained through nitrosation of the urea corresponding to cystamine is then possible. Furthermore, a new synth