(S,S)-()-2,3-Dimethoxy-1,4-bis(dimethylamino)butane

≥97%

Reagent Code: #69097
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CAS Number 26549-21-3

science Other reagents with same CAS 26549-21-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.31 g/mol
Formula C₁₀H₂₄N₂O₂
badge Registry Numbers
MDL Number MFCD00063598
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where stereoselectivity is crucial. It is often employed in the formation of carbon-carbon and carbon-heteroatom bonds, enhancing the efficiency and selectivity of the process. Its application extends to the synthesis of complex organic molecules, including pharmaceuticals, where precise control over the stereochemistry is essential. Additionally, it is used in the development of enantiomerically pure compounds, which are important in the production of active pharmaceutical ingredients (APIs) and fine chemicals.

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Test Parameter Specification
Appearance Colorless to light orange to yellow clear liquid
Purity 96.5-100
Infrared spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿3,120.00
inventory 1g
10-20 days ฿10,120.00

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(S,S)-()-2,3-Dimethoxy-1,4-bis(dimethylamino)butane
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This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where stereoselectivity is crucial. It is often employed in the formation of carbon-carbon and carbon-heteroatom bonds, enhancing the efficiency and selectivity of the process. Its application extends to the synthesis of complex organic molecules, including pharmaceuticals, where precise control over the stereochemistry is essential. Additionally, it is used in the development of enantiomer

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where stereoselectivity is crucial. It is often employed in the formation of carbon-carbon and carbon-heteroatom bonds, enhancing the efficiency and selectivity of the process. Its application extends to the synthesis of complex organic molecules, including pharmaceuticals, where precise control over the stereochemistry is essential. Additionally, it is used in the development of enantiomerically pure compounds, which are important in the production of active pharmaceutical ingredients (APIs) and fine chemicals.

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