CAS 38235-77-7
:(+)-Benzylphenethylamine
Description:
(+)-Benzylphenethylamine, with the CAS number 38235-77-7, is an organic compound that belongs to the class of phenethylamines. It features a benzyl group attached to a phenethylamine backbone, which contributes to its structural complexity and potential biological activity. This compound is characterized by its chiral nature, existing as a specific enantiomer, which can influence its pharmacological properties. Typically, it is a colorless to pale yellow liquid or solid, depending on its purity and form. (+)-Benzylphenethylamine may exhibit stimulant effects and has been studied for its potential applications in various fields, including medicinal chemistry and neuroscience. Its interactions with neurotransmitter systems, particularly in relation to dopamine and norepinephrine, make it of interest in research on mood and cognitive function. However, due to its structural similarity to other psychoactive substances, it is essential to handle it with caution and be aware of regulatory considerations surrounding its use and distribution.
Formula:C15H17N
InChI:InChI=1S/C15H17N/c1-13(15-10-6-3-7-11-15)16-12-14-8-4-2-5-9-14/h2-11,13,16H,12H2,1H3/t13-/m1/s1
InChI key:InChIKey=ZYZHMSJNPCYUTB-CYBMUJFWSA-N
SMILES:[C@@H](NCC1=CC=CC=C1)(C)C2=CC=CC=C2
Synonyms:- (+)-Benzylphenethylamine
- (+)-N-Benzyl-1-phenylethylamine
- (+)-N-Benzyl-α-phenylethylamine
- (1R)-N-(cyclohexylmethyl)-1-phenylethanaminium
- (R)-(+)-N-Benzyl-1-phenylethylamine
- (R)-(+)-N-Benzyl-α-methylbenzylamine
- (R)-Benzyl(α-methylbenzyl)amine
- (R)-N-(α-Methylbenzyl)-N-benzylamine
- (R)-N-Benzyl-1-phenyl-1-ethylamine
- (R)-N-Benzyl-1-phenylethan-1-amine
- (R)-N-Benzyl-1-phenylethanamine
- (R)-N-Benzyl-N-(-methylbenzyl)amine
- (R)-N-Benzyl-N-α-methylbenzylamine
- (αR)-α-Methyl-N-(phenylmethyl)benzenemethanamine
- Benzenemethanamine, α-methyl-N-(phenylmethyl)-, (R)-
- Benzenemethanamine, α-methyl-N-(phenylmethyl)-, (αR)-
- Benzyl((R)-1-phenylethyl)amine
- N-Benzyl((R)-1-phenylethyl)amine
- N-Benzyl-(R)-α-methylbenzylamine
- N-Benzyl-1-phenylethanamine
- N-[(R)-1-Phenylethyl]benzylamine
- See more synonyms
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Found 7 products.
(R)-(+)-N-Benzyl-1-phenylethylamine
CAS:Formula:C15H17NPurity:>98.0%(GC)Color and Shape:Colorless to Light yellow clear liquidMolecular weight:211.31(R)-(+)-N-Benzyl-1-Phenylethylamine
CAS:Formula:C15H17NPurity:96%Color and Shape:LiquidMolecular weight:211.3022(R)-(+)-N-Benzyl-1-phenylethylamine
CAS:<p>(R)-(+)-N-Benzyl-1-phenylethylamine</p>Formula:C15H17NPurity:97%Color and Shape: clear. yellow liquidMolecular weight:211.30g/molR)-(+)-N-Benzyl-1-phenylethylamine
CAS:Controlled Product<p>Applications R)-(+)-N-Benzyl-1-phenylethylamine, can be used as an both starting and intermediate in the chemical synthesis of pharmaceutical compounds. It is a starting material for the preparation of (R)-3-Aminobutan-1-ol (A602105).<br>References Johns, B. et al.: J. Med. Chem., 56, 5901 (2013);<br></p>Formula:C15H17NColor and Shape:NeatMolecular weight:211.3(R)-(+)-N-Benzyl-1-phenylethylamine
CAS:Formula:C15H17NPurity:97%Color and Shape:LiquidMolecular weight:211.308Ref: 10-F012696
1g12.00€5g13.00€10g14.00€1kg297.00€25g20.00€50g31.00€100g50.00€250g102.00€500g171.00€(R)-(+)-N-Benzyl-1-phenylethylamine
CAS:<p>(R)-(+)-N-Benzyl-1-phenylethylamine is an enantiomer of phenylethylamine. It is a chiral, vinylic amine that can be used to produce catalytic asymmetric Grignard reactions. The synthesis of this compound starts with the addition of benzyl chloride to 1-phenylethylamine. This reaction produces (R)-(+)-N-benzyl-1-phenylethylamine as the major product and its corresponding bisulfate salt as the minor product. This compound has been shown to be an anti HIV drug in a number of studies, which may be due to its ability to inhibit reverse transcriptase and/or prevent viral entry into cells.</p>Formula:C15H17NPurity:Min. 95%Color and Shape:Colourless To Pale Yellow LiquidMolecular weight:211.3 g/mol






