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

CAS: 132335-44-5

Ref. 3D-ID58105

Produktinformation

• Name: (S)-3-(Dimethylamino)-1-(2-thienyl)propan-1-ol
• Synonyme: (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

Beschreibung

(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.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 185.29 g/mol
• Formel: C₉H₁₅NOS
• Reinheit: Min. 95%