(1R,2R)-Methyl 2-(4-Bromobenzoyl)Cyclopentanecarboxylate

98%

Reagent Code: #231764
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CAS Number 791594-14-4

science Other reagents with same CAS 791594-14-4

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Weight 311.17 g/mol
Formula C₁₄H₁₅BrO₃
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Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and central nervous system agents. Its chiral cyclopentane backbone allows for selective interactions in biological systems, making it valuable in asymmetric synthesis. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the presence of reactive functional groups that can be further modified. Also utilized in the preparation of enzyme inhibitors where stereochemistry plays a critical role in activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,030.00
inventory 250mg
10-20 days ฿31,720.00
inventory 1g
10-20 days ฿82,820.00

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(1R,2R)-Methyl 2-(4-Bromobenzoyl)Cyclopentanecarboxylate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and central nervous system agents. Its chiral cyclopentane backbone allows for selective interactions in biological systems, making it valuable in asymmetric synthesis. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the presence of reactive functional groups that can be further modified. Also utilized in the preparation of enzyme inhibi

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and central nervous system agents. Its chiral cyclopentane backbone allows for selective interactions in biological systems, making it valuable in asymmetric synthesis. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the presence of reactive functional groups that can be further modified. Also utilized in the preparation of enzyme inhibitors where stereochemistry plays a critical role in activity.

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