CAS ID | 2627-86-3 |
---|---|
IUPAC Name | (1S)-1-phenylethanamine |
Molecular Formula | C8H11N |
Molecular Weight | |
SMILES | CC(C1=CC=CC=C1)N |
CAS ID | 2627-86-3 |
---|---|
IUPAC Name | (1S)-1-phenylethanamine |
Molecular Formula | C8H11N |
Molecular Weight | |
SMILES | CC(C1=CC=CC=C1)N |
75818 |
Synonym: s—1-phenylethylamine, s-1-phenylethanamine, 1s-1-phenylethanamine, s—alpha-methylbenzylamine, s-1-phenylethylamine, l–alpha-methylbenzylamine, l-alpha-methylbenzylamine, s-alpha-methylbenzenemethanamine, –alpha-phenethylamine, l—1-phenylethylamine
Boiling Point | 84°C |
Color | Yellow |
UN Number | 2922 |
Formula Weight | 121.18 |
Physical Form | Clear Liquid at 20°C |
Chemical Name or Material | (S)-(-)-1-Phenylethylamine |
Our scientists have experience in all research areas, including life science, material science, chemical custom synthesis, chromatography, analytical science, and many others.
S-1-Phenylethylamine is appreciated for its chiral amine structure, making it a key precursor in producing enantiomerically pure chemicals. Its phenylethylamine chemical structure makes it useful in asymmetric synthesis applications.
The phenylethylamine chemical structure leads to S-1-Phenylethylamine's distinct reactivity. Its amine group and phenyl ring allow various pharmaceutical, agrochemical, and materials science research uses.
When purchasing phenethylamine, check that it satisfies quality standards and regulatory criteria. S-1-Phenylethylamine should have a proven phenylethylamine chemical structure and be well purified to facilitate advanced research and manufacturing.
S-1-Phenylethylamine's phenylethylamine chemical structure makes it suitable for bespoke chemical formulations. Researchers frequently purchase phenethylamine for custom synthesis projects requiring high enantiomeric purity.
S-1-phenylethylamine has a unique stereochemical structure that provides enhanced selectivity in chemical processes. This distinguishing feature of its phenylethylamine chemical structure promotes its popularity in research and development.