156004-66-9

Basic information

• Product Name: (S)-N,3-diMethyl-1-(pyrrolidin-1-yl)butan-2-aMine
• Synonyms: (S)-N,3-diMethyl-1-(pyrrolidin-1-yl)butan-2-aMine
• CAS NO: 156004-66-9
• Molecular Formula: C₁₀H₂₂N₂
• Molecular Weight: 170.29508
• Mol File: 156004-66-9.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (S)-N,3-diMethyl-1-(pyrrolidin-1-yl)butan-2-aMine(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-N,3-diMethyl-1-(pyrrolidin-1-yl)butan-2-aMine(156004-66-9)
• EPA Substance Registry System: (S)-N,3-diMethyl-1-(pyrrolidin-1-yl)butan-2-aMine(156004-66-9)

Safety Data

• Hazardous Substances Data: 156004-66-9(Hazardous Substances Data)

Usage

Description

(S)-N,3-diMethyl-1-(pyrrolidin-1-yl)butan-2-aMine, with the molecular formula C10H21N, is a chiral amine characterized by the presence of a non-superimposable mirror image. This unique property allows it to exist as two distinct enantiomers, which can exhibit different effects in biological systems. Its potential applications in the pharmaceutical industry make it a molecule of significant interest for drug development and synthesis.

Uses

Used in Pharmaceutical Industry:
(S)-N,3-diMethyl-1-(pyrrolidin-1-yl)butan-2-aMine is used as a building block for the synthesis of various drugs and pharmaceutical products. Its chirality plays a crucial role in drug development, as the different enantiomers can have distinct biological activities and effects.
Used in Chemical Intermediates:
In the chemical industry, (S)-N,3-diMethyl-1-(pyrrolidin-1-yl)butan-2-aMine may serve as a valuable chemical intermediate for the synthesis of other complex organic compounds, contributing to the development of novel materials and products.

Upstream product

• 56414-68-7 benzyl N-<(1S)-2-methyl-1-(1-pyrrolidinylcarbonyl)propyl>carbamate 
• 1149-26-4 (S)-N-(benzyloxycarbonyl)valine 

Downstream Products

• 1380102-10-2 (S)-1-(2-(4-chloro-N-methylbenzamido)-3-methylbutyl)pyrrolidinium chloride 
• 136328-64-8 ICI 197067 
• 136328-65-9 N-Methyl-N-((S)-2-methyl-1-pyrrolidin-1-ylmethyl-propyl)-2-phenyl-acetamide 
• 136328-72-8 N-Methyl-N-((S)-2-methyl-1-pyrrolidin-1-ylmethyl-propyl)-2-phenoxy-acetamide 
• 136328-69-3 N-Methyl-N-((S)-2-methyl-1-pyrrolidin-1-ylmethyl-propyl)-2-(4-trifluoromethyl-phenyl)-acetamide 
• 115200-03-8 2-(3,4-Difluoro-phenyl)-N-methyl-N-((S)-2-methyl-1-pyrrolidin-1-ylmethyl-propyl)-acetamide 
• 136328-73-9 N-Methyl-N-((S)-2-methyl-1-pyrrolidin-1-ylmethyl-propyl)-2-phenylsulfanyl-acetamide 
• 136328-68-2 N-Methyl-N-((S)-2-methyl-1-pyrrolidin-1-ylmethyl-propyl)-2-(4-nitro-phenyl)-acetamide 
• 136328-66-0 2-(3-Chloro-phenyl)-N-methyl-N-((S)-2-methyl-1-pyrrolidin-1-ylmethyl-propyl)-acetamide 
• 136328-71-7 N-Methyl-N-((S)-2-methyl-1-pyrrolidin-1-ylmethyl-propyl)-3-phenyl-propionamide 
• 136328-67-1 2-(4-Chloro-phenyl)-N-methyl-N-((S)-2-methyl-1-pyrrolidin-1-ylmethyl-propyl)-acetamide 
• 136328-70-6 2-(4-Methoxy-phenyl)-N-methyl-N-((S)-2-methyl-1-pyrrolidin-1-ylmethyl-propyl)-acetamide 

Relevant articles and documents

Enantioselective deprotonation of cyclohexene oxide to (R)-2-cyclohexen- 1-ol

The reaction of cyclohexene oxide with homochiral lithium amides, prepared from (S)-phenylglycine and (S)-valine has been studied and (R)-2-cyclohexen- 1-ol 3 was prepared in a maximum of 72% ee. The optical purity was determined by 1H NMR measurement of the α-methoxy-α-(trifluoromethyl)phenyl acetic acid (MTPA) derivative of the corresponding alcohol.