CAS ID | 3886-69-9 |
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IUPAC Name | (1R)-1-phenylethanamine |
Molecular Formula | C8H11N |
Molecular Weight | |
SMILES | CC(C1=CC=CC=C1)N |
CAS ID | 3886-69-9 |
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IUPAC Name | (1R)-1-phenylethanamine |
Molecular Formula | C8H11N |
Molecular Weight | |
SMILES | CC(C1=CC=CC=C1)N |
643189 |
Synonym: r-1-phenylethanamine, r-+-1-phenylethylamine, 1r-1-phenylethanamine, r-1-phenylethylamine, d-alpha-methylbenzylamine, 1r-1-phenylethan-1-amine, r-+-alpha-methylbenzylamine, r-alpha-methylbenzenemethanamine, unii-v022zk8gz5, r-alfa-methylbenzylamine
Color | Yellow |
Boiling Point | 85°C |
UN Number | 2922 |
Formula Weight | 121.18 |
Physical Form | Clear Liquid at 20°C |
Chemical Name or Material | (R)-(+)-1-Phenylethylamine |
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The chemical formula for 1-phenylethylamine is C8H11N, an organic compound. Because of its structural resemblance to natural neurotransmitters and its potential biological action, this chiral amine is frequently used in pharmaceutical and chemical research.
1-phenylethylamine is extensively used in chemical synthesis, especially in the pharmaceutical and fine chemical industries. Due to its chiral characteristics, it is used as an intermediate in the development of physiologically active chemicals and in asymmetric synthesis.
Specific plant and animal tissues do contain 1-phenylethylamine. Its exact biological role is unknown, although it may play a role in neuromodulation and act as a trace amine in humans.
1-phenylethylamine is an invaluable component in the creation of new medications. The interaction of its derivatives with neurotransmitter pathways makes them promising candidates for treating neurological diseases.
1-phenylethylamine is utilized widely in industries such as pharmaceuticals, agrochemicals, and speciality chemicals for the synthesis of intermediates, fine chemicals, and physiologically active compounds. It plays an essential role in both academic and commercial chemistry.