(S)-(-)-1-Phenylethylamine | 2627-86-3

Additional information

CAS ID

2627-86-3

IUPAC Name

(1S)-1-phenylethanamine

Molecular Formula

C8H11N

Molecular Weight

SMILES

CC(C1=CC=CC=C1)N

General Information

Additional information

CAS ID

2627-86-3

IUPAC Name

(1S)-1-phenylethanamine

Molecular Formula

C8H11N

Molecular Weight

SMILES

CC(C1=CC=CC=C1)N

Description

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

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(S)-(-)-1-Phenylethylamine | 2627-86-3 FAQS

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.