Interesting facts
Interesting Facts About 2-(4-Fluorophenyl)ethanamine
2-(4-Fluorophenyl)ethanamine, often referred to in scientific circles for its intriguing properties and potential applications, is an organic compound that has garnered attention in the field of medicinal chemistry. Here are some fascinating aspects of this compound:
- Pharmacological Relevance: This compound is structurally related to various psychoactive agents. Its amine functional group is pivotal in interacting with biological systems, and studies suggest potential implications in the treatment of mood disorders.
- Fluorination Impact: The presence of fluorine in its structure can alter the lipophilicity and metabolic stability, making compounds like 2-(4-fluorophenyl)ethanamine interesting candidates for drug development. Fluorine atoms can enhance the bioavailability of drugs.
- Research Interest: Ongoing research is exploring the effects of this compound on neurotransmitter systems in the brain. Specifically, its interaction with serotonin and dopamine receptors piques the interest of scientists looking to develop new therapeutic agents.
- Synthetic Pathways: The synthesis of 2-(4-fluorophenyl)ethanamine can be achieved through various methods, which often involve nucleophilic substitution reactions. Understanding these pathways not only reveals valuable information about amine chemistry but also aids in developing efficient synthesis techniques for related compounds.
- Analytical Techniques: Characterization of this compound often involves analytical techniques such as NMR and mass spectrometry, which are crucial for understanding its properties and verifying its structure in laboratory settings.
As scientists delve deeper into the complexities of 2-(4-fluorophenyl)ethanamine, its contribution to the world of organic synthesis and medicinal chemistry continues to unfold, highlighting the vital intersection of structure and function in chemistry.
Synonyms
4-Fluorophenethylamine
1583-88-6
2-(4-Fluorophenyl)ethanamine
2-(4-fluorophenyl)ethylamine
Benzeneethanamine, 4-fluoro-
P-fluorophenethylamine
2-(4-fluorophenyl)ethan-1-amine
2-(4-fluoro-phenyl)-ethylamine
MFCD00134208
(p-fluorophenyl)ethylamine
S7W3CQD7N7
EINECS 216-435-6
2-(p-fluorophenyl)ethylamine
4-(2-aminoethyl)fluorobenzene
2-(4-fluorophenyl)-ethylamine
CHEMBL217315
4-FLUOROBENZENEETHANAMINE
DTXSID70166400
4-Fluorophenylethylamine
4-fluoro-phenethylamine
4-fluorophenethyl amine
4-fluorophenylethyl amine
UNII-S7W3CQD7N7
(4-fluorobenzyl)methylamine
SCHEMBL5414
4-Fluorophenethylamine, 99%
4-fluoro-beta-phenylethylamine
DTXCID9088891
2-(4-Fluorophenyl)ethanamine #
2-(4-fluoro-phenyl) ethyl amine
HMS1728I10
1-Amino-2-(4-fluorophenyl)ethane
BBL013000
BDBM50241087
GEO-01418
STL163864
AKOS000120310
AB03730
CS-W018312
FF38252
TS-01809
DB-064219
F0829
NS00082953
EN300-18739
Z90122126
2-(4-Fluoro-phenyl)-ethylamine;4-fluorophenylethylamine
F2190-0530
216-435-6
Solubility of 2-(4-fluorophenyl)ethanamine (C8H10FN)
2-(4-fluorophenyl)ethanamine, commonly known for its intriguing properties, exhibits notable solubility characteristics influenced by its molecular structure. Understanding the solubility of this compound is essential for various applications, particularly in pharmaceutical research and chemical synthesis.
Key Points on Solubility:
As a rule of thumb in chemical behavior, “Like Dissolves Like” applies here: the combination of amine and phenyl functional groups positions 2-(4-fluorophenyl)ethanamine favorably in environments where polar interactions are prevalent. Thus, both researchers and practitioners should anticipate its variable solubility depending on the chosen solvent or surrounding conditions.