Interesting facts
Interesting Facts About 1,3-Dichloropropan-2-one
1,3-Dichloropropan-2-one, a valuable compound in the realm of organic chemistry, showcases a unique structure and diverse applications. Here are some fascinating insights about this compound:
- Versatile Intermediate: This compound serves as an intermediate in the synthesis of various pharmaceuticals, making it integral to the pharmaceutical industry.
- Chlorinated Compounds: As a chlorinated ketone, it exhibits distinct chemical properties that can be exploited in various reactions.
- Synthesis Method: It can be synthesized through different methods, commonly involving the chlorination of propan-2-one, offering chemists multiple pathways to obtain this compound.
- Environmental Considerations: Like many chlorinated organic compounds, 1,3-dichloropropan-2-one necessitates careful handling due to potential environmental impacts; it is crucial to conduct risk assessments in its use.
- Research Applications: This compound is often utilized in research settings to study reaction mechanisms and the effects of chlorination on organic compounds.
The significance of 1,3-dichloropropan-2-one in chemical research and industry cannot be overstated. As chemists continue to explore its properties and reactions, this compound remains an essential subject of study.
Synonyms
1,3-Dichloroacetone
534-07-6
1,3-dichloropropan-2-one
1,3-Dichloropropanone
Bis(chloromethyl) ketone
s-Dichloroacetone
Bis(chloromethyl)ketone
2-Propanone, 1,3-dichloro-
BISCHLOROMETHYL KETONE
Acetone, 1,3-dichloro
1,3-Dichloroacetona
Dichloro-1,3 acetone
CCRIS 1942
1,3-Dichloroacetona [Spanish]
Dichloro-1,3 acetone [French]
HSDB 6391
NSC 8745
EINECS 208-585-6
UNII-UFH8559WS5
BRN 0605456
DTXSID2021577
NSC-8745
DTXCID001577
CHEBI:156485
1,3-DICHLOROACETONE [MI]
4-01-00-03219 (Beilstein Handbook Reference)
BISCHLOROMETHYL KETONE [HSDB]
1,3-Dichloroacetona (Spanish)
Dichloro-1,3 acetone (French)
208-585-6
inchi=1/c3h4cl2o/c4-1-3(6)2-5/h1-2h
sunmbrgcanloeg-uhfffaoysa-n
1,3-Dichloro-2-propanone
sym-Dichloroacetone
1,3-DICHLORO-PROPAN-2-ONE
chloromethyl ketone
UFH8559WS5
.alpha.,.alpha.'-Dichloroacetone
CAS-534-07-6
alpha,gamma-Dichloroacetone
1,3-dichloracetone
1,3 dichloroacetone
1.3-dichloroacetone
1 ,3-dichloroacetone
1,3-di-chloroacetone
1,3-dichloro acetone
1,3-dichloro-acetone
CHLOROMETYL-KETONE
2-Propanone,3-dichloro-
alpha,alpha'-Dichloroacetone
1,3-dichloro -2-propanone
SCHEMBL30570
CHEMBL1231783
.alpha.,.gamma.-Dichloroacetone
1,3-Dichloroacetone, >=95%
1,3-bis(chloranyl)propan-2-one
NSC8745
Tox21_201433
Tox21_302809
MFCD00000937
STL163858
AKOS000120303
NCGC00249044-01
NCGC00256565-01
NCGC00258984-01
AS-39890
PD194063
1,3-Dichloroacetone [UN2649] [Poison]
D0401
NS00006201
EN300-20702
A829568
doi:10.14272/SUNMBRGCANLOEG-UHFFFAOYSA-N.1
Q4917164
F0001-1383
Solubility of 1,3-Dichloropropan-2-one
1,3-Dichloropropan-2-one, with the chemical formula C3H4Cl2O, exhibits interesting solubility characteristics that are noteworthy for various applications. This compound is primarily soluble in organic solvents.
Solubility Characteristics:
Overall, 1,3-Dichloropropan-2-one serves as a significant solvent and reagent in the laboratory due to its unique solubility profile. As it is often employed in synthesis, understanding its solubility can guide researchers in selecting appropriate solvents for successful reactions.