(1R,2R)-rel-trans-1,2-Cyclopentanediol

97%

Reagent Code: #230051
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CAS Number 5057-99-8

science Other reagents with same CAS 5057-99-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 102.13 g/mol
Formula C₅H₁₀O₂
badge Registry Numbers
MDL Number MFCD00082582
thermostat Physical Properties
Melting Point 46-50°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its rigid cyclopentane backbone and two hydroxyl groups in a trans configuration make it valuable for designing stereoselective reactions. Commonly employed in the development of antiviral and antitumor agents, where the spatial orientation of functional groups is critical. Also utilized in asymmetric synthesis and as a precursor in the preparation of complex natural products. The compound’s ability to act as a diol linker enhances its utility in medicinal chemistry and drug design.

Available Sizes & Pricing

Size Availability Unit Price Quantity
200mg
10-20 days ฿180.00
1g
10-20 days ฿750.00
5g
10-20 days ฿3,600.00
(1R,2R)-rel-trans-1,2-Cyclopentanediol
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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 hydroxyl groups in a trans configuration make it valuable for designing stereoselective reactions. Commonly employed in the development of antiviral and antitumor agents, where the spatial orientation of functional groups is critical. Also utilized in asymmetric synthesis and as a precursor in the preparation of complex natural products. The compound’s ability to act
Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its rigid cyclopentane backbone and two hydroxyl groups in a trans configuration make it valuable for designing stereoselective reactions. Commonly employed in the development of antiviral and antitumor agents, where the spatial orientation of functional groups is critical. Also utilized in asymmetric synthesis and as a precursor in the preparation of complex natural products. The compound’s ability to act as a diol linker enhances its utility in medicinal chemistry and drug design.
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