(1R,2R)-1,2-Bis(4-fluorophenyl)ethane-1,2-diamine dihydrochloride

97%

Reagent Code: #231806
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CAS Number 1055301-10-4

science Other reagents with same CAS 1055301-10-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 321.19 g/mol
Formula C₁₄H₁₆Cl₂F₂N₂
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its rigid, stereospecific structure makes it valuable in asymmetric synthesis, where it helps control the spatial arrangement of atoms in drug molecules. Commonly employed in the preparation of intermediates for HIV and hepatitis C treatments. Also utilized in catalysis and as a ligand in transition metal-catalyzed reactions to produce enantiomerically pure compounds.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿8,270.00
250mg
10-20 days ฿14,040.00
1g
10-20 days ฿41,040.00
(1R,2R)-1,2-Bis(4-fluorophenyl)ethane-1,2-diamine dihydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its rigid, stereospecific structure makes it valuable in asymmetric synthesis, where it helps control the spatial arrangement of atoms in drug molecules. Commonly employed in the preparation of intermediates for HIV and hepatitis C treatments. Also utilized in catalysis and as a ligand in transition metal-catalyzed reactions to produce enantiomerically pure com

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its rigid, stereospecific structure makes it valuable in asymmetric synthesis, where it helps control the spatial arrangement of atoms in drug molecules. Commonly employed in the preparation of intermediates for HIV and hepatitis C treatments. Also utilized in catalysis and as a ligand in transition metal-catalyzed reactions to produce enantiomerically pure compounds.

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