Interesting facts
Introduction to 3-Chloropropylbenzene
3-Chloropropylbenzene, an aromatic compound with interesting properties, serves as a key building block in organic synthesis. Known for its unique structure, this compound features a benzene ring substituted with a propyl group and a chlorine atom, leading to its notable reactivity.
Key Facts About 3-Chloropropylbenzene
- Industrial Relevance: 3-Chloropropylbenzene is frequently used in the production of various chemicals, including pharmaceuticals and agrochemicals. Its chlorinated nature makes it a significant intermediate in chemical reactions.
- Synthetic Applications: Chemists often utilize 3-chloropropylbenzene in nucleophilic substitution reactions, allowing for the introduction of diverse functional groups into the molecule, which expands its utility in synthetic organic chemistry.
- Environmental Considerations: Like many chlorinated compounds, 3-chloropropylbenzene poses environmental challenges. The presence of chlorine can lead to persistent organic pollutants, necessitating careful handling and disposal practices.
- Structural Characteristics: The positioning of the chlorine atom at the 3-position (meta) relative to the propyl group contributes to the compound's reactivity profile, influencing how it interacts with other substances in chemical reactions.
- Reacting at the Right Temperature: As a scientist, one must consider the temperature and reaction conditions when working with 3-chloropropylbenzene, as these can significantly affect its reactivity and the efficiency of desired transformations.
Conclusion
In summary, 3-chloropropylbenzene is more than just a component in organic chemistry; it represents a crucial intersection of practical applications and theoretical exploration. As researchers continue to delve into its properties and reactions, this compound remains an important subject of study within the field of chemistry.
Synonyms
1-Chloro-3-phenylpropane
(3-CHLOROPROPYL)BENZENE
104-52-9
3-Phenylpropyl chloride
3-chloropropylbenzene
Benzene, (3-chloropropyl)-
3-Chloro-1-phenylpropane
3-Phenyl-1-chloropropane
.gamma.-Chloropropylbenzene
.gamma.-Phenylpropyl chloride
E2L2KN77K8
EINECS 203-210-2
MFCD00001001
NSC 16939
NSC-16939
(3-chloro-propyl)-benzene
AI3-23863
DTXSID10146206
ALVERINE CITRATE IMPURITY A [EP IMPURITY]
Benzene, (chloropropyl)-
gamma-Chloropropylbenzene
ALVERINE CITRATE IMPURITY A (EP IMPURITY)
gamma-Phenylpropyl chloride
3-Phenylpropylchloride
3-Phenylpropanyl chloride
3-(phenyl)propyl chloride
UNII-E2L2KN77K8
SCHEMBL432616
CHEMBL1234093
DTXCID1068697
XZBXAYCCBFTQHH-UHFFFAOYSA-
1-Chloro-3-phenylpropane, 99%
NSC16939
STL268874
AKOS000121307
CS-W016261
GS-3136
SY048978
DB-027396
NS00023307
P1262
EN300-21262
S12344
Q27462696
F0001-0090
InChI=1/C9H11Cl/c10-8-4-7-9-5-2-1-3-6-9/h1-3,5-6H,4,7-8H2
203-210-2
Alverine Citrate Imp. A (EP); Alverine Imp. A (EP); 1-Chloro-3-phenylpropane; Alverine Citrate Impurity A; Alverine Impurity A
LT1
Solubility of 3-chloropropylbenzene
3-chloropropylbenzene, with the chemical formula C10H11Cl, exhibits interesting solubility characteristics primarily due to its molecular structure. The compound features a benzene ring with a propyl group and a chlorine atom, which influences its interaction with various solvents.
When exploring the solubility of 3-chloropropylbenzene, consider the following aspects:
To summarize, the solubility of 3-chloropropylbenzene can be best described as follows:
Understanding these solubility traits is essential for applications in organic chemistry and related fields, allowing for effective manipulation in various chemical processes.