Interesting facts
Interesting Facts about 2-Bromoethylbenzene
2-Bromoethylbenzene, an important organic compound, holds a notable position in the field of synthetic chemistry. This compound is frequently utilized as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, showcasing its versatility. Here are some intriguing aspects of 2-Bromoethylbenzene:
- Substituted Aromatic Compound: As a bromo derivative of ethylbenzene, it showcases how substituents can dramatically affect the chemical reactivity and properties of aromatic compounds.
- Reactivity: The bromine atom in 2-Bromoethylbenzene serves as a great leaving group, facilitating nucleophilic substitution reactions, which are pivotal in building complex organic molecules.
- Applications in Synthesis: This compound is often used to produce other functionalized compounds, making it invaluable in organic synthesis. Some applications include:
- Synthesis of pharmaceuticals that target various diseases
- Preparation of specialty chemicals and agrochemical products
- Environmental Consideration: Like many brominated compounds, 2-Bromoethylbenzene must be handled with care due to potential environmental impacts and safety concerns, especially regarding its persistence and effects on ecosystems.
In the realm of organic chemistry, compounds like 2-Bromoethylbenzene are essential due to their roles in developing new materials, medicines, and chemical processes. As we delve deeper into the intricate world of organic compounds, each molecule tells a story of chemical interactions and potential innovations.
Synonyms
(2-BROMOETHYL)BENZENE
103-63-9
Phenethyl bromide
2-Bromoethylbenzene
Phenylethyl bromide
2-Phenylethyl bromide
1-Bromo-2-phenylethane
Benzene, (2-bromoethyl)-
2-Phenethyl bromide
2-Phenyl-1-bromoethane
beta-Bromoethylbenzene
.beta.-Bromoethylbenzene
Bromoethylbenzene
Benzene, (bromoethyl)-
2-phenylbromoethane
Phenylethyl bromide (VAN)
Benzene, bromoethyl-
NSC 33926
ar-Monobromoethylbenzene
phenethylbromide
1-phenyl-2-bromoethane
HSDB 5352
EINECS 203-130-8
beta-Phenethyl bromide
DTXSID1033876
AI3-11264
.beta.-Phenethyl bromide
(2-bromo-ethyl)-benzene
NSC-33926
.beta.-Phenylethyl bromide
31620-80-1
96O442668X
DTXCID9013876
NSC 6534
EINECS 250-734-2
MFCD00000240
FENTANYL CITRATE IMPURITY I [EP IMPURITY]
2-phenyl ethyl bromide
FENTANYL CITRATE IMPURITY I (EP IMPURITY)
2-(BROMOETHYL)BENZENE
phenethyl bromine
phenylethylbromide
bromoethyl benzene
2-bromoethylbenzen
2Phenethyl bromide
UNII-96O442668X
(bromoethyl)benzene
1Bromo2phenylethane
2Phenyl1bromoethane
3-Bromoethylbenzene
Benzene, bromoethyl
betaBromoethylbenzene
2-phenylethylbromide
2phenylethyl bromide
(2bromoethyl)benzene
2-bromoethyl benzene
2-bromoethyl-benzene
2-phenyl-ethylbromid
(2-bromethyl)benzene
arMonobromoethylbenzene
beta-phenylethylbromide
(2-phenyl)bromoethane
1-(bromoethyl)benzene
2-phenyl-ethyl bromide
beta-Phenylethyl bromide
(2-bromo ethyl)benzene
(2-bromoethyl) benzene
2-(bromo-ethyl)benzene
2-(bromoethyl)-benzene
(2-Bromoethyl)-benzene
Benzene, (2bromoethyl)
(2-brom-ethyl)-benzene
1-(2-bromoethyl)benzene
2-phenyl-1-ethyl bromide
SCHEMBL1552
1-(2-bromo-ethyl)-benzene
MLS001055470
(2-Bromoethyl)benzene, 98%
CHEMBL1340745
DTXSID201057323
HMS3039C09
HY-Y0199
NSC33926
STR01487
Tox21_200102
BBL027290
STL197570
AKOS005216002
CS-W019955
FB12171
NCGC00090999-01
NCGC00090999-02
NCGC00257656-01
BP-30043
CAS-103-63-9
FENTANYL IMPURITY L [EP IMPURITY]
SMR001227201
DB-002310
DB-020722
DS-009931
B0594
NS00021460
S12296
(2-Bromoethyl)benzene, purum, >=97.0% (GC)
2-Phenylethyl bromide;Fentanyl Related Compound A
A800773
A929174
Q4596916
F0001-0079
250-734-2
Solubility of 2-bromoethylbenzene
2-bromoethylbenzene, with the chemical formula C8H9Br, is of particular interest when it comes to solubility characteristics. Here are some key points to consider:
In summary, while 2-bromoethylbenzene is relatively insoluble in water, it demonstrates a greater affinity for organic solvents. Understanding solubility behavior is essential for practical applications in chemical synthesis and industrial processes, as it can impact reaction efficiency and product recovery.