2627-86-3
2627-86-3
Chemical Structure
(S)-(-)-1-Phenylethanamine
Synonym(s): S-(-)-α-Phenylethylamine;L-(-)-α-Methylbenzylamine
- CAS No.: 2627-86-3
- Formula:C8H11N
- Molecular Weight:121.18
IUPAC Name: (S)-1-phenylethan-1-amine
InChIKey: RQEUFEKYXDPUSK-ZETCQYMHSA-N
SMILES: N[C@@H](C)C1=CC=CC=C1
Biological Activity: (S)-(-)-1-Phenylethanamine (S-(-)-α-Phenylethylamine; L-(-)-α-Methylbenzylamine) is a S-isomer of 1-Phenylethanamine (HY-W012848). (S)-(-)-1-Phenylethanamine can be used as a pharmaceutical intermediate for the synthesis of various active compounds[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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(S)-(-)-1-Phenylethanamine | 99.84% | (S)-(-)-1-Phenylethanamine (S-(-)-α-Phenylethylamine; L-(-)-α-Methylbenzylamine) is a S-isomer of 1-Phenylethanamine (HY-W012848). (S)-(-)-1-Phenylethanamine can be used as a pharmaceutical intermediate for the synthesis of various active compounds. | ||||||||||||||||||||
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References
- [1]. Kaiser DG, et al. Isomeric inversion of ibuprofen (R)-enantiomer in humans. J Pharm Sci. 1976 Feb;65(2):269-73. [Content Brief]
- [2]. Reddy CN, et al. 7S,15R-Stereoisomer of phenylethylamino derivative of colchicine exhibits potent in-vitro and in-vivo anti-cancer activity against prostate Cancer: Assessing the impact of stereochemistry on biological activity. Bioorg Chem. 2025 Apr;157:108262. [Content Brief]
Keywords
