(R)-1-(6-Bromopyridin-2-yl)ethan-1-ol

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Reagent Code: #231871
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CAS Number 138983-04-7

science Other reagents with same CAS 138983-04-7

blur_circular Chemical Specifications

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Weight 2025 g/mol
Formula C₇H₈BrNO
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors and other bioactive molecules. Its bromine functionality allows for further cross-coupling reactions, enabling structural diversification. The presence of a stereogenic center makes it valuable in asymmetric synthesis, where stereochemistry plays a critical role in biological activity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid pyridine core and modifiable hydroxyl group.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,540.00
inventory 100mg
10-20 days ฿9,030.00
inventory 250mg
10-20 days ฿14,740.00
inventory 500mg
10-20 days ฿23,920.00
inventory 1g
10-20 days ฿36,760.00

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(R)-1-(6-Bromopyridin-2-yl)ethan-1-ol
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Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors and other bioactive molecules. Its bromine functionality allows for further cross-coupling reactions, enabling structural diversification. The presence of a stereogenic center makes it valuable in asymmetric synthesis, where stereochemistry plays a critical role in biological activity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) stud

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors and other bioactive molecules. Its bromine functionality allows for further cross-coupling reactions, enabling structural diversification. The presence of a stereogenic center makes it valuable in asymmetric synthesis, where stereochemistry plays a critical role in biological activity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid pyridine core and modifiable hydroxyl group.

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