(S)-Pyrrolidine-2-carbonitrile 4-methylbenzenesulfonate

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Reagent Code: #38641
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CAS Number 204387-54-2

science Other reagents with same CAS 204387-54-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 268.3320 g/mol
Formula C₁₂H₁₆N₂O₃S
badge Registry Numbers
MDL Number MFCD12827848
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block for the preparation of pharmaceuticals. Its structure, featuring a pyrrolidine ring and a nitrile group, makes it valuable for constructing complex molecules with specific stereochemistry. It is often employed in the synthesis of chiral amines, which are crucial intermediates in the production of various drugs, including those targeting central nervous system disorders and cardiovascular diseases. Additionally, its tosylate group enhances reactivity, facilitating further chemical modifications. The compound’s chiral nature also makes it useful in asymmetric synthesis, enabling the creation of enantiomerically pure compounds.

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Test Parameter Specification
Appearance White to Off-White Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,797.00

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(S)-Pyrrolidine-2-carbonitrile 4-methylbenzenesulfonate
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This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block for the preparation of pharmaceuticals. Its structure, featuring a pyrrolidine ring and a nitrile group, makes it valuable for constructing complex molecules with specific stereochemistry. It is often employed in the synthesis of chiral amines, which are crucial intermediates in the production of various drugs, including those targeting central nervous system disorders and cardiovascular disease

This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block for the preparation of pharmaceuticals. Its structure, featuring a pyrrolidine ring and a nitrile group, makes it valuable for constructing complex molecules with specific stereochemistry. It is often employed in the synthesis of chiral amines, which are crucial intermediates in the production of various drugs, including those targeting central nervous system disorders and cardiovascular diseases. Additionally, its tosylate group enhances reactivity, facilitating further chemical modifications. The compound’s chiral nature also makes it useful in asymmetric synthesis, enabling the creation of enantiomerically pure compounds.

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