Rel-(1R,2R)-2-(4-Fluorophenyl)-4-Oxocyclopentane-1-Carboxylic Acid

97%

Reagent Code: #231532
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CAS Number 104201-85-6

science Other reagents with same CAS 104201-85-6

blur_circular Chemical Specifications

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Weight 222.21 g/mol
Formula C₁₂H₁₁FO₃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key chiral intermediate in the synthesis of prostaglandin analogs, particularly in the production of ophthalmic drugs for treating glaucoma. Its stereochemistry enables selective biological activity, making it valuable in developing medications that reduce intraocular pressure. The compound's structure allows efficient coupling in multi-step syntheses of active pharmaceutical ingredients, especially in agents like latanoprost or similar prostaglandin derivatives. Its fluorinated aromatic group enhances metabolic stability and target binding affinity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,360.00
Rel-(1R,2R)-2-(4-Fluorophenyl)-4-Oxocyclopentane-1-Carboxylic Acid
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Used as a key chiral intermediate in the synthesis of prostaglandin analogs, particularly in the production of ophthalmic drugs for treating glaucoma. Its stereochemistry enables selective biological activity, making it valuable in developing medications that reduce intraocular pressure. The compound's structure allows efficient coupling in multi-step syntheses of active pharmaceutical ingredients, especially in agents like latanoprost or similar prostaglandin derivatives. Its fluorinated aromatic group

Used as a key chiral intermediate in the synthesis of prostaglandin analogs, particularly in the production of ophthalmic drugs for treating glaucoma. Its stereochemistry enables selective biological activity, making it valuable in developing medications that reduce intraocular pressure. The compound's structure allows efficient coupling in multi-step syntheses of active pharmaceutical ingredients, especially in agents like latanoprost or similar prostaglandin derivatives. Its fluorinated aromatic group enhances metabolic stability and target binding affinity.

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