CAS 598-19-6
:2-Propen-1-ol, 2-bromo-
Description:
2-Propen-1-ol, 2-bromo- is an organic compound characterized by its structure, which features a bromine atom attached to the second carbon of a propene chain with a hydroxyl group (alcohol functional group) at the first carbon. This compound is a colorless to pale yellow liquid with a distinctive odor. It is soluble in water due to the presence of the hydroxyl group, which allows for hydrogen bonding. The presence of the bromine atom introduces reactivity, making it a useful intermediate in organic synthesis, particularly in reactions such as nucleophilic substitution and elimination. The compound can undergo polymerization, especially under acidic conditions, leading to the formation of larger molecular structures. Safety considerations are important, as it may be harmful if inhaled or ingested, and appropriate handling procedures should be followed. Overall, 2-Propen-1-ol, 2-bromo- is a versatile compound in organic chemistry with applications in various chemical reactions and synthesis pathways.
Formula:C3H5BrO
InChI:InChI=1S/C3H5BrO/c1-3(4)2-5/h5H,1-2H2
InChI key:InChIKey=MDFFZNIQPLKQSG-UHFFFAOYSA-N
SMILES:C(CO)(Br)=C
Synonyms:- 2-Bromo-1-propen-3-ol
- 2-Bromo-2-propen-1-ol
- 2-Bromoprop-2-En-1-Ol
- 2-Propen-1-Ol, 2-Bromo-
- 2-Bromoallyl alcohol
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Found 4 products.
2-Bromoallyl Alcohol
CAS:Formula:C3H5BrOPurity:>97.0%(GC)Color and Shape:Colorless to Yellow to Orange clear liquidMolecular weight:136.982-Bromoallyl alcohol
CAS:<p>2-Bromoallyl alcohol is a halogenated aromatic hydrocarbon that is an analyte in the chemical analysis of soil. It is also used as a reagent for the debromination of 2-bromopropane and as a dehalogenating agent for the removal of bromine from organic compounds. 2-Bromoallyl alcohol can be distilled at high temperatures, but it will volatilize if heated to 80°C or higher. It has been reported that 2-bromoallyl alcohol was found to be present in all replicates analyzed. The recovery of this compound ranged from 83% to 114%. 2-Bromoallyl alcohol is used as a reagent in organic synthesis, such as in palladium catalyzed couplings with boronic acids and esters. This compound may also be used to synthesize N-(2-hydroxyethyl)hydroxylamines by reacting with sodium hydroxide</p>Formula:C3H5BrOPurity:Min. 95%Molecular weight:136.98 g/mol



