(S)-1-(3-bromopyridin-2-yl)ethanol

95%

Reagent Code: #235983
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Alias RAS Inhibitors
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CAS Number 317845-81-1

science Other reagents with same CAS 317845-81-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.05 g/mol
Formula C₇H₈BrNO
badge Registry Numbers
MDL Number MFCD26860013
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active molecules. Its chiral center and functional groups allow for selective reactions, making it valuable in asymmetric synthesis. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in drug efficacy and safety. Also utilized in research settings for the construction of complex heterocyclic compounds due to the presence of the bromopyridine moiety, which enables further cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,950.00
inventory 5g
10-20 days ฿7,980.00
inventory 25g
10-20 days ฿36,210.00
(S)-1-(3-bromopyridin-2-yl)ethanol
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active molecules. Its chiral center and functional groups allow for selective reactions, making it valuable in asymmetric synthesis. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in drug efficacy and safety. Also utilized in research settings for the construction of complex heterocy

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active molecules. Its chiral center and functional groups allow for selective reactions, making it valuable in asymmetric synthesis. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in drug efficacy and safety. Also utilized in research settings for the construction of complex heterocyclic compounds due to the presence of the bromopyridine moiety, which enables further cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations.

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