4-(Benzhydryloxy)-4-Oxobutanoic Acid

98%

Reagent Code: #154069
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CAS Number 128925-50-8

science Other reagents with same CAS 128925-50-8

blur_circular Chemical Specifications

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Weight 284.31 g/mol
Formula C₁₇H₁₆O₄
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It serves as a building block in the development of antihistamines and anticholinergic agents due to the presence of the benzhydryl moiety, which is common in central nervous system-active drugs. The carboxylic acid group allows for further functionalization, enabling peptide coupling or esterification to modify drug solubility and bioavailability. Also employed in the synthesis of prodrugs where controlled release is achieved through ester derivatives. Its structure supports research in medicinal chemistry for designing molecules with improved metabolic stability and receptor selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,030.00

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4-(Benzhydryloxy)-4-Oxobutanoic Acid
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It serves as a building block in the development of antihistamines and anticholinergic agents due to the presence of the benzhydryl moiety, which is common in central nervous system-active drugs. The carboxylic acid group allows for further functionalization, enabling peptide coupling or esterification to modify drug solubility and bioavailability. Also employed in the synthesis of prodrugs where co

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It serves as a building block in the development of antihistamines and anticholinergic agents due to the presence of the benzhydryl moiety, which is common in central nervous system-active drugs. The carboxylic acid group allows for further functionalization, enabling peptide coupling or esterification to modify drug solubility and bioavailability. Also employed in the synthesis of prodrugs where controlled release is achieved through ester derivatives. Its structure supports research in medicinal chemistry for designing molecules with improved metabolic stability and receptor selectivity.

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