(S)-3-(Dimethylamino)-1-(2-thienyl)propan-1-ol

CAS : 132335-44-5

Ref. 3D-ID58105

Informations sur le produit

• Nom: (S)-3-(Dimethylamino)-1-(2-thienyl)propan-1-ol
• Synonymes: (S)-1-b-Hydroxy-1-(2-thienyl)-3-dimethylaminopropaneS-(-)-N,N-Dimethyl-3-hydroxy-3-(2-thienyl)propanamine, (1S)-3-(Dimethylamino)-1-(2-thienyl)-1-propanol, (1S)-3-(Dimethylamino)-1-(thiophen-2-yl)propan-1-ol, (1S)-3-(dimethylamino)-1-thiophen-2-ylpropan-1-ol, (S)-(-)-N,N-dimethyl-3-hydroxy-3-(2-thienyl)propylamine, (S)-(-)-N-Dimethyl-3-Hydroxy-3-(2-Thienyl)-Propanamine, (S)-(-)-alpha-methyl-1-naphthalenemethhanol, (S)-1-Beta-Hydroxy-1-(2-Thienyl)-3-Dimethylaminopropane, (S)-1-Hydroxy-1-(2-Thienyl)-3-Dimethylaminopropane, (S)-2-[3-(Dimethylamino)-1-hydroxypropyl]thiophene, (S)-3-(Dimethylamino)-1-(2-Thienyl)-1-Propanol, (S)-3-Dimethylamino-1-(thiophen-2-yl)-propan-1-ol, (S)-N,N-Dimethyl-3-(2-thienyl)-3-hydroxypropanamine, (S)-N,N-Dimethyl-3-hydroxy-3-(2-thienyl)-1-propylamine, (S)-N,N-dimethyl-3-hydroxy-3-(2-thienyl)-2-propanamine, (S)-alpha-[2-(Dimethylamino)ethyl]-2-thiophenemethanol, (S)-α-[2-(Dimethylamino)ethyl]-2-thiophenemethanol, (αS)-α-[2-(Dimethylamino)ethyl]-2-thiophenemethanol, 2-Thiophenemethanol, α-[2-(dimethylamino)ethyl]-, (S)-, 2-Thiophenemethanol, α-[2-(dimethylamino)ethyl]-, (αS)-, Duloxetine intermediate AA, S-(-)-N,N-Dimethyl-3-Hydroxy-(2-Thienol)Propanamine, S-(-)-N,N-Dimethyl-3-hydroxy-3-(2-thienyl)-1-propanamine, S-(-)-N,N-DIMETHYL-3-HYDR0XY-3-(2-THENYL)PROPANAMINE, (S)-(-)-N,N-Dimethyl-3-hydroxy-3-(2-thienyl)propanamine, S-(-)-N,N-Dimethyl-3-Hydroxy-3-(2-thienyl)propanamine, S)-(-)-N,N-dimethyl-3-hydroxy-3-(2-thienyl)-propanamine, (S)-(-)-N,N-Dimethyl-3-hydroxy-3-(2-thienyl) propanamine

Description

(S)-3-(Dimethylamino)-1-(2-thienyl)propan-1-ol is a polymerase chain reaction (PCR) reagent that is used as a building block for the synthesis of five membered ring lactams and dihedral polymers. This compound is synthesized by chemoenzymatic coupling of propanamine with trifluoroacetic acid in the presence of methyl groups, followed by catalytic hydrogenation to yield the desired product. The asymmetric synthesis of this compound was achieved through chiral resolution using NMR spectroscopy.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 185.29 g/mol
• Formule: C₉H₁₅NOS
• Degré de pureté: Min. 95%