Interesting facts
Interesting Facts About 2,3-Dichloroprop-1-ene
2,3-Dichloroprop-1-ene is an intriguing organic compound with significant applications and properties that make it worthy of study. Here are some fascinating facts about this compound:
- Structure and Bonds: The molecular structure of 2,3-dichloroprop-1-ene features a double bond between the first and second carbon atoms, contributing to its reactivity and unique chemical behavior.
- Chirality: One of the noteworthy aspects of 2,3-dichloroprop-1-ene is its potential for chirality. Depending on the orientation of the chlorine atoms attached to the carbon chain, it can exist as two distinct stereoisomers, which can have different chemical properties.
- Industrial Uses: This compound is utilized in various industrial applications, including its role as an intermediate in the synthesis of other chemicals. It's particularly valued for its reactive double bond, which can participate in further chemical reactions.
- Environmental Concerns: Like many chlorinated compounds, 2,3-dichloroprop-1-ene raises important environmental considerations. Its potential as a groundwater contaminant underscores the need for careful handling and monitoring.
- Safety Precautions: Researchers working with this compound should be aware of its health and safety implications. Proper protective gear and laboratory protocols are essential to minimize exposure and ensure safety.
In summary, 2,3-Dichloroprop-1-ene may seem simple at first glance, but it presents a wealth of interesting chemical properties and challenges that make it a fascinating compound for chemists and researchers alike. As the study of organic compounds continues to expand, 2,3-dichloroprop-1-ene will undoubtedly remain a topic of interest in both academic and industrial settings.
Synonyms
2,3-DICHLORO-1-PROPENE
2,3-Dichloropropene
78-88-6
2,3-dichloroprop-1-ene
2-Chloroallyl chloride
2,3-Dichloropropylene
1-Propene, 2,3-dichloro-
Propene, 2,3-dichloro-
1,2-Dichloro-2-propene
Propylene, 2,3-dichloro
CCRIS 956
HSDB 5222
EINECS 201-153-8
NSC 60520
UNII-370TNK5I41
BRN 1361491
DTXSID6025012
2,3-Dichloro-propene
AI3-14619
370TNK5I41
NSC-60520
2,3-Dichloropropene-(1)
DTXCID605012
EC 201-153-8
DICHLORO-1-PROPENE, 2,3-
2,3-DICHLORO-1-PROPENE [HSDB]
2,?3-?Dichloro-?1-?propene
3-dichloro-propene
NSC60520
MFCD00000943
1,2Dichloro2propene
2,3Dichloro1propene
2,3Dichloropropylene
2Chloroallyl chloride
Propene, 2,3dichloro
Propylene, 2,3dichloro
1Propene, 2,3dichloro
1,2-dichloroprop-2-ene
2,3-dichloro-prop-1-ene
WLN: G1YGU1
Pesticide Code: 042005
SCHEMBL78819
PROPENE,2,3-DICHLORO
CHEMBL156075
2,3-bis(chloranyl)prop-1-ene
1-PROPENE,2,3-DICHLORO
2,3-DICHLORO-1-PROPANE
2,3-Dichloro-1-propene, 98%
AAA07888
Tox21_200640
AKOS000121539
CAS-78-88-6
NCGC00091735-01
NCGC00091735-02
NCGC00258194-01
BS-43822
DB-056341
D0406
NS00005333
EN300-21166
D97733
A839523
Q27256607
Solubility of 2,3-Dichloroprop-1-ene
2,3-Dichloroprop-1-ene, with the chemical formula C3H4Cl2, exhibits intriguing solubility properties influenced by its unique structure and functional groups.
When discussing solubility, several key points emerge:
In the realm of practical applications, understanding the solubility of 2,3-dichloroprop-1-ene is crucial for its utilization in various chemical processes, where the solvent choice can significantly affect reactivity and product yield.
Ultimately, solubility can be categorized thus:
As with many organic compounds, the interplay between molecular structure and solvent characteristics leads to the intricate solubility behavior observed in 2,3-dichloroprop-1-ene.