35420-95-2

Usage

Uses

Used in Laboratory Research:
2-Bromoethyl ethyl sulfide is used as a laboratory reagent for conducting experiments and research in the field of organic chemistry. Its reactivity as an alkylating agent makes it a valuable tool for synthesizing new compounds and studying chemical reactions.
Used in Organic Synthesis:
In the realm of organic synthesis, 2-Bromoethyl ethyl sulfide serves as an intermediate, contributing to the formation of more complex organic molecules. Its role in synthesis processes is crucial for the development of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Chemical Warfare:
Although its use is highly regulated and discouraged under international law, 2-Bromoethyl ethyl sulfide has been known to be used as a blister agent in warfare. Exposure to this chemical can result in severe irritation and damage to the skin, eyes, and respiratory system, highlighting the need for stringent protective measures during its handling, storage, and disposal.

InChI:InChI=1/C4H9BrS/c1-2-6-4-3-5/h2-4H2,1H3

Upstream product

• 110-77-0 2-(ethylsulfanyl)ethanol 
• 75-08-1 ethanethiol 
• 74-85-1 ethene 
• 7789-60-8 phosphorus tribromide 
• 25561-30-2 N,O-Bis(trimethylsilyl)trifluoroacetamide 
• 693-07-2 2-Chloroethyl ethyl sulfide 
• 106-93-4 ethylene dibromide 

Downstream Products

• 64036-98-2 ethyl-(2-ethylsulfanyl-ethyl)-(2-dimethoxyphosphorylsulfanyl-ethyl)-sulfonium ; bromide 
• 860726-94-9 (2-ethylsulfanyl-ethyl)-phenyl-arsinic acid 
• 114841-74-6 S-ethyl-S-(2-bromo-ethyl)-N-(toluene-4-sulfonyl)-sulfimide 
• 126-75-0 Demeton-S 
• 1133166-68-3 C₂₈H₄₅N₆O₁₀PS 

Relevant academic research and scientific papers

ABSORBENT COMPOSITIONS INCLUDING AMINO-SILOXANES

An absorbent composition including an amino-siloxane is presented. The amino- siloxane includes structure (I): wherein R1 is independently at each occurrence a C1-C6 aliphatic or aromatic radical; R2 is independ

Difluoro- and trifluoro diazoalkanes-complementary approaches in batch and flow and their application in cycloaddition reactions

Herein we report on applications of fluorinated diazoalkanes in cycloaddition reactions, with the emphasis on studying subtle differences between diverse fluorinated diazo compounds. These differences led to two major synthetic protocols in batch and flow that allow the safe and scalable synthesis of fluoroalkyl-, sulfone-substituted pyrazolines.

METHOD OF TREATING CANCER WITH A COMBINATION OF BENZYLIDENEGUANIDINE DERIVATIVES AND CHEMOTHERAPEUTIC AGENT.

The present invention relates to a composition for use in treating a glioma or ameliorating the effects of a glioma, particularly glioblastoma, wherein said composition comprises a first active agent selected from the group consisting of a compound of for

O-ALKYL-BENZYLIDENEGUANIDINE DERIVATIVES AND THERAPEUTIC USE FOR THE TREATMENT OF DISORDERS ASSOCIATED AN ACCUMULATION OF MISFOLDED PROTEINS

The present invention relates to a compound of formula (I), or a tautomer and/or a pharmaceutically acceptable salt thereof Formula (I), and its uses to treat a disorder associated with protein misfolding stress and in particular with an accumulation of m

Reaction Products and Process of 2-Chloroethyl Ethyl Sulfide in Microemulsion Media

The reaction of 2-chloroethyl ethyl sulfide was investigated in several oil-in-water microemulsions. The reaction products were identified by GC/MS, NMR, and LC/MS, and the reaction process was monitored by measuring peak height of reaction products and 2-chloroethyl ethyl sulfide with time by 1H NMR spectroscopy. The result showed that 2-chloroethyl ethyl sulfide degraded to 2-hydroxyethyl ethyl sulfide, cyclic sulfonium ion, open chain sulfonium chloro ion and sulfonium hydroxyl ion, and the reaction proceeded via a cyclic sulfonium ion intermediate. Based on the NMR results, a pseudoternary model was established for the reaction process of 2-chloroethyl ethyl sulfide in microemulsion.

Synthesis, characterization, and heterobimetallic cooperation in a titanium-chromium catalyst for highly branched polyethylenes

A heterobimetallic catalyst, {Ti - Cr}, consisting of a constrained-geometry titanium olefin polymerization center (CGCEtTi) covalently linked to a chromium bis(thioether)amine ethylene trimerization center (SNSCr) was synthesized and fully characterized. In ethylene homopolymerizations it affords linear low-density polyethylene with molecular weights as high as 460 kg·mol-1 and exclusively n-butyl branches in conversion-insensitive densities of ～18 branches/1000 carbon atoms, which are ～17 and ～3 times (conversion-dependent), respectively, those achieved by tandem mononuclear CGCEtTi and SNSCr catalysts under identical reaction conditions.