(R)-(+)-1-(p-Tolyl)ethylamine

CAS : 4187-38-6

Ref. 3D-FT60267

Informations sur le produit

• Nom: (R)-(+)-1-(p-Tolyl)ethylamine
• Synonymes: (R)-(+)-4-(1-Aminoethyl)toluene, (+)-1-(4-Methylphenyl)ethylamine, (+)-1-(p-Tolyl)ethylamine, (+)-p-Methyl-α-phenylethylamine, (1R)-1-(4-Methylphenyl)ethan-1-amine, (1R)-1-(4-Methylphenyl)ethanamine, (R)-(+)-1-(4-Methylphenyl)ethylamine, (R)-(+)-4-Methyl-α-methylbenzylamine, (R)-(+)-p,α-Dimethylbenzylamine, (R)-(+)-α,4-Dimethylbenzylamine, (R)-1-(p-Methylphenyl)ethylamine, (R)-1-(p-Tolyl)ethanamine, (R)-4-Tolylethylamine, (αR)-α,4-Dimethylbenzenemethanamine, Benzenemethanamine, α,4-dimethyl-, (R)-, Benzenemethanamine, α,4-dimethyl-, (αR)-, Benzylamine, p,α-dimethyl-, (+)-, Tolylethylamine, [(R)-(+)-1-(4-Methylphenyl)ethyl]amine

Description

(R)-(+)-1-(p-Tolyl)ethylamine (TPA) is a chiral molecule that has been studied in the context of crystallographic analysis and optimization. The crystal structure of TPA was determined by X-ray diffraction analysis and found to have a hydrogen bond between the amine group and one of the carbonyl groups. This hydrogen bond is thought to be important for stabilizing the TPA molecule, as it is observed in many other molecules with similar structures. The (S)-(+)-enantiomer of TPA was synthesized from an enantiopure precursor, which resulted in an efficient method for obtaining this desired form of the molecule. The pharmacological properties and applications of TPA are still being explored, but it has been shown to have anti-inflammatory effects.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 135.21 g/mol
• Formule: C₉H₁₃N
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C9H13N/c1-7-3-5-9(6-4-7)8(2)10/h3-6,8H,10H2,1-2H3/t8-/m1/s1
• Code InChI: InChIKey=UZDDXUMOXKDXNE-MRVPVSSYSA-N
• SMILES: Cc1ccc([C@@H](C)N)cc1