35420-95-2

Basic information

• Product Name: 2-BROMOETHYL ETHYL SULFIDE
• Synonyms: 2-BROMOETHYL ETHYL SULFIDE
• CAS NO: 35420-95-2
• Molecular Formula: C₄H₉BrS
• Molecular Weight: 169.08
• Mol File: 35420-95-2.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 57 °C
• Flash Point: 62 °C
• Appearance: /
• Density: 1.389g/cm³
• Vapor Pressure: 1.31mmHg at 25°C
• Refractive Index: 1.508
• CAS DataBase Reference: 2-BROMOETHYL ETHYL SULFIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BROMOETHYL ETHYL SULFIDE(35420-95-2)
• EPA Substance Registry System: 2-BROMOETHYL ETHYL SULFIDE(35420-95-2)

Safety Data

• Hazardous Substances Data: 35420-95-2(Hazardous Substances Data)

Usage

General Description

2-Bromoethyl ethyl sulfide is a chemical compound with the molecular formula C4H9BrS. It is a colorless to pale yellow liquid with a pungent odor, and it is a reactive alkylating agent. This chemical is used as a laboratory reagent and intermediate in organic synthesis. It is also known for its use as a warfare agent, specifically as a blister agent. Exposure to 2-Bromoethyl ethyl sulfide can cause severe irritation and damage to the skin, eyes, and respiratory system. Protective measures should be taken when handling this compound, and it should be stored and disposed of properly according to regulations.

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

• 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 
• 64036-98-2 ethyl-(2-ethylsulfanyl-ethyl)-(2-dimethoxyphosphorylsulfanyl-ethyl)-sulfonium ; bromide 

Relevant articles and documents

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.

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.