Dimethyl (1R,3S)-cyclopentane-1,3-dicarboxylate

98%

Reagent Code: #229289
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CAS Number 190137-08-7

science Other reagents with same CAS 190137-08-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.21 g/mol
Formula C₉H₁₄O₄
thermostat Physical Properties
Boiling Point 240.8±15.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.135±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its rigid cyclopentane backbone and ester functional groups allow for selective transformations, making it valuable in asymmetric synthesis. Commonly employed in the preparation of prostaglandin analogs and other medicinally relevant molecules where stereochemistry plays a critical role in biological activity. The compound’s defined stereochemistry (1R,3S) enables precise control in ring-forming reactions and side-chain elaborations, particularly in research targeting central nervous system agents and anti-inflammatory drugs.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,830.00
250mg
10-20 days ฿4,800.00
Dimethyl (1R,3S)-cyclopentane-1,3-dicarboxylate
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Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its rigid cyclopentane backbone and ester functional groups allow for selective transformations, making it valuable in asymmetric synthesis. Commonly employed in the preparation of prostaglandin analogs and other medicinally relevant molecules where stereochemistry plays a critical role in biological activity. The compound’s defined stereochemistry (1R,3S) enables precise control in ring-forming reactio

Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its rigid cyclopentane backbone and ester functional groups allow for selective transformations, making it valuable in asymmetric synthesis. Commonly employed in the preparation of prostaglandin analogs and other medicinally relevant molecules where stereochemistry plays a critical role in biological activity. The compound’s defined stereochemistry (1R,3S) enables precise control in ring-forming reactions and side-chain elaborations, particularly in research targeting central nervous system agents and anti-inflammatory drugs.

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