(1R,2R)-Cyclopentane-1,2-diamine dihydrochloride

98%

Reagent Code: #228751
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CAS Number 1030390-38-5

science Other reagents with same CAS 1030390-38-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.08 g/mol
Formula C₅H₁₄Cl₂N₂
badge Registry Numbers
MDL Number MFCD10000875
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its rigid cyclopentane backbone and defined stereochemistry make it valuable in asymmetric synthesis, particularly in the development of catalysts and ligands for enantioselective reactions. Commonly employed in the preparation of protease inhibitors and other medicinal agents where stereochemical control is critical. Also utilized in the design of novel amine-containing molecules for drug discovery due to its stability and functional group compatibility.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,660.00
inventory 250mg
10-20 days ฿19,180.00
inventory 1g
10-20 days ฿55,610.00
(1R,2R)-Cyclopentane-1,2-diamine dihydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its rigid cyclopentane backbone and defined stereochemistry make it valuable in asymmetric synthesis, particularly in the development of catalysts and ligands for enantioselective reactions. Commonly employed in the preparation of protease inhibitors and other medicinal agents where stereochemical control is critical. Also utilized in the design of novel amine-containing molecules for drug discovery due

Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its rigid cyclopentane backbone and defined stereochemistry make it valuable in asymmetric synthesis, particularly in the development of catalysts and ligands for enantioselective reactions. Commonly employed in the preparation of protease inhibitors and other medicinal agents where stereochemical control is critical. Also utilized in the design of novel amine-containing molecules for drug discovery due to its stability and functional group compatibility.

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