(R)-N1,N1-dimethyl-4-(phenylthio)butane-1,3-diamine

98%

Reagent Code: #232202
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CAS Number 870812-32-1

science Other reagents with same CAS 870812-32-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.37 g/mol
Formula C₁₂H₂₀N₂S
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MDL Number MFCD27930860
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of central nervous system agents. Its structural features make it valuable in asymmetric synthesis, where the (R)-enantiomer contributes to stereoselective reactions. Commonly employed in the preparation of serotonin and norepinephrine reuptake inhibitors, it plays a role in optimizing the pharmacokinetic profile of active drug substances. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its amine and thioether functionalities.

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inventory 100mg
10-20 days ฿14,420.00

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(R)-N1,N1-dimethyl-4-(phenylthio)butane-1,3-diamine
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Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of central nervous system agents. Its structural features make it valuable in asymmetric synthesis, where the (R)-enantiomer contributes to stereoselective reactions. Commonly employed in the preparation of serotonin and norepinephrine reuptake inhibitors, it plays a role in optimizing the pharmacokinetic profile of active drug substances. Also utilized in medicinal chemistry for structure-ac

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of central nervous system agents. Its structural features make it valuable in asymmetric synthesis, where the (R)-enantiomer contributes to stereoselective reactions. Commonly employed in the preparation of serotonin and norepinephrine reuptake inhibitors, it plays a role in optimizing the pharmacokinetic profile of active drug substances. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its amine and thioether functionalities.

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