(R)-(+)-1-(4-Methoxyphenyl)ethylamine

CAS: 22038-86-4

Ref. 3D-FM60261

Produktinformation

• Name: (R)-(+)-1-(4-Methoxyphenyl)ethylamine
• Synonyme: (R)-(+)-4-Methoxy-α-methylbenzylamine, ((R)-α-Methyl-p-Methoxybenzyl)amine, (+)-1-(4-Methoxyphenyl)ethylamine, (+)-p-Methoxy-α-phenylethylamine, (+)-α-(p-Methoxyphenyl)ethylamine, (1R)-1-(4-methoxyphenyl)ethanamine, (R)-(+)-4-Methoxyphenylethylamine, (R)-1-(4-Methoxyphenyl)ethanamine, (R)-1-(p-Methoxyphenyl)ethylamine, (R)-p-Methoxy-alpha-methylbenzylamine, (αR)-4-Methoxy-α-methylbenzenemethanamine, Benzenemethanamine, 4-methoxy-α-methyl-, (R)-, Benzenemethanamine, 4-methoxy-α-methyl-, (αR)-, Benzylamine, p-methoxy-α-methyl-, (R)-(+)-, R(+)-1-(4-Methoxyphenyl)Ethyla, [(1R)-1-[4-(Methyloxy)phenyl]ethyl]amine

Beschreibung

(R)-(+)-1-(4-Methoxyphenyl)ethylamine is a stereoselective chemical that binds to the protein target of cytosolic calcium, hydrochloric acid, and hiv infection. The stereoselective nature of (R)-(+)-1-(4-Methoxyphenyl)ethylamine makes it an efficient method for amines. Protein synthesis is a biological function of (R)-(+)-1-(4-Methoxyphenyl)ethylamine. This chemical is synthesized by the transfer reactions of glyoxal and trifluoroacetic acid. The synthetic pathway starts with the biosynthesis of (S)-(-)-2-methoxyacetophenone and ends with the conversion to (R)-(+)-1-(4-methoxyphenyl)ethylamine.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 151.21 g/mol
• Formel: C₉H₁₃NO
• Reinheit: Min. 95%
• Farbe/Form: Clear Liquid