(R)-1-(4-(Methylthio)phenyl)ethanamine hydrochloride

95%

Reagent Code: #232373
fingerprint
CAS Number 1391401-54-9

science Other reagents with same CAS 1391401-54-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.73 g/mol
Formula C₉H₁₄ClNS
badge Registry Numbers
MDL Number MFCD16294237
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its enantiomeric purity makes it valuable for creating active ingredients in antidepressants and antipsychotic drugs. The compound's amine functionality allows for easy derivatization, enabling its incorporation into more complex molecules. It is also employed in asymmetric synthesis and as a resolving agent for racemic mixtures. Due to the presence of the methylthio group, it can participate in further functional group transformations, expanding its utility in medicinal chemistry and drug discovery processes.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿3,610.00
250mg
10-20 days ฿8,320.00
1g
10-20 days ฿24,940.00
(R)-1-(4-(Methylthio)phenyl)ethanamine hydrochloride
No image available

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its enantiomeric purity makes it valuable for creating active ingredients in antidepressants and antipsychotic drugs. The compound's amine functionality allows for easy derivatization, enabling its incorporation into more complex molecules. It is also employed in asymmetric synthesis and as a resolving agent for racemic mixtures. Due to the presence of the methylthio grou

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its enantiomeric purity makes it valuable for creating active ingredients in antidepressants and antipsychotic drugs. The compound's amine functionality allows for easy derivatization, enabling its incorporation into more complex molecules. It is also employed in asymmetric synthesis and as a resolving agent for racemic mixtures. Due to the presence of the methylthio group, it can participate in further functional group transformations, expanding its utility in medicinal chemistry and drug discovery processes.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...