(3S)-N-(1-Methylethyl)-3-pyrrolidinamine

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Reagent Code: #236647
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CAS Number 854140-09-3

science Other reagents with same CAS 854140-09-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 128.215 g/mol
Formula C₇H₁₆N₂
badge Registry Numbers
MDL Number MFCD18837107
thermostat Physical Properties
Boiling Point 175 °C at 760 mmHg
inventory_2 Storage & Handling
Density 0.90 g/cm3
Storage Room temperature

description Product Description

Used as a chiral building block in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the formation of complex amines found in bioactive molecules. Commonly employed in the production of central nervous system (CNS) agents and as an intermediate in the synthesis of receptor agonists or antagonists. Also utilized in the preparation of catalysts for asymmetric reactions due to its stereogenic center and amine functionality.

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inventory 1g
10-20 days ฿41,400.00

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(3S)-N-(1-Methylethyl)-3-pyrrolidinamine
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Used as a chiral building block in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the formation of complex amines found in bioactive molecules. Commonly employed in the production of central nervous system (CNS) agents and as an intermediate in the synthesis of receptor agonists or antagonists. Also utilized in the preparation of catalysts for asymmetric reactions due to its stereogenic cente

Used as a chiral building block in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the formation of complex amines found in bioactive molecules. Commonly employed in the production of central nervous system (CNS) agents and as an intermediate in the synthesis of receptor agonists or antagonists. Also utilized in the preparation of catalysts for asymmetric reactions due to its stereogenic center and amine functionality.

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