cis-Cyclopentane-1,2-diamine dihydrochloride

95%

Reagent Code: #163165
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CAS Number 310872-08-3

science Other reagents with same CAS 310872-08-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.08 g/mol
Formula C₅H₁₄Cl₂N₂
badge Registry Numbers
MDL Number MFCD28411589
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its rigid cyclopentane backbone and two adjacent amine groups make it valuable in asymmetric synthesis and catalyst design. Commonly employed in the development of chiral ligands and organocatalysts for enantioselective reactions. Also utilized in medicinal chemistry for constructing peptidomimetics and nitrogen-containing heterocycles. The dihydrochloride salt form enhances stability and solubility, facilitating handling and use in aqueous or polar organic solvents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,680.00
inventory 250mg
10-20 days ฿3,970.00
inventory 1g
10-20 days ฿7,590.00
inventory 5g
10-20 days ฿28,730.00

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cis-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 two adjacent amine groups make it valuable in asymmetric synthesis and catalyst design. Commonly employed in the development of chiral ligands and organocatalysts for enantioselective reactions. Also utilized in medicinal chemistry for constructing peptidomimetics and nitrogen-containing heterocycles. The dihydrochloride salt form enhances stability and solubility, fa

Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its rigid cyclopentane backbone and two adjacent amine groups make it valuable in asymmetric synthesis and catalyst design. Commonly employed in the development of chiral ligands and organocatalysts for enantioselective reactions. Also utilized in medicinal chemistry for constructing peptidomimetics and nitrogen-containing heterocycles. The dihydrochloride salt form enhances stability and solubility, facilitating handling and use in aqueous or polar organic solvents.

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