CAS 35420-95-2
:1-bromo-2-(ethylsulfanyl)ethane
Description:
1-Bromo-2-(ethylsulfanyl)ethane is an organic compound characterized by the presence of a bromine atom and an ethylsulfanyl group attached to a two-carbon ethane backbone. Its molecular structure features a bromine substituent at the first carbon and an ethylthio group at the second carbon, which contributes to its reactivity and potential applications in organic synthesis. This compound is typically a colorless to pale yellow liquid with a distinctive odor. It is soluble in organic solvents but has limited solubility in water due to its hydrophobic ethylsulfanyl group. The presence of the bromine atom makes it a good candidate for nucleophilic substitution reactions, allowing for the introduction of various functional groups. Additionally, the ethylsulfanyl group can participate in further chemical transformations, making this compound useful in the synthesis of more complex molecules. Safety precautions should be observed when handling this compound, as it may pose health risks if inhaled or ingested.
Formula:C4H9BrS
InChI:InChI=1/C4H9BrS/c1-2-6-4-3-5/h2-4H2,1H3
SMILES:CCSCCBr
Synonyms:- 2-Bromoethyl ethyl sulfide
- Ethane, 1-Bromo-2-(Ethylthio)-
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Found 2 products.
2-Bromoethyl ethyl sulfide
CAS:Formula:C4H9BrSPurity:98.0%Color and Shape:LiquidMolecular weight:169.082-Bromoethyl ethyl sulfide
CAS:<p>2-Bromoethyl ethyl sulfide (2BEES) is a colorless liquid with a strong, sulfur-like odor. It is soluble in water, but not in organic solvents. 2BEES is a nucleophilic reagent that reacts with electrophiles at the carbon atom adjacent to the electron-donating group. The reaction of 2BEES with an electron-deficient aromatic ring can lead to substitution or elimination reactions. 2BEES has a boiling point of 108°C and its spectral data corresponds to that of chlorine. The activation energy for this reaction is 29 kJ/mol.</p>Formula:C4H9BrSPurity:Min. 95%Molecular weight:169.08 g/mol

