(S)-3-Bromo-2-(1-methoxyethyl)pyridine

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Reagent Code: #236907
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CAS Number 2641451-44-5

science Other reagents with same CAS 2641451-44-5

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active pyridine derivatives. Its stereochemistry makes it valuable for asymmetric synthesis, where it helps introduce specific chirality into target molecules. Commonly employed in the preparation of neuroactive compounds and enzyme inhibitors due to the reactivity of the bromo group and the structural influence of the methoxyethyl side chain. Also utilized in cross-coupling reactions such as Suzuki or Negishi couplings to build complex heterocyclic systems in medicinal chemistry research.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿560.00
1g
10-20 days ฿1,680.00
5g
10-20 days ฿5,880.00
10g
10-20 days ฿9,860.00
25g
10-20 days ฿22,550.00
50g
10-20 days ฿44,000.00
100g
10-20 days ฿76,800.00

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(S)-3-Bromo-2-(1-methoxyethyl)pyridine
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active pyridine derivatives. Its stereochemistry makes it valuable for asymmetric synthesis, where it helps introduce specific chirality into target molecules. Commonly employed in the preparation of neuroactive compounds and enzyme inhibitors due to the reactivity of the bromo group and the structural influence of the methoxyethyl side chain. Also utilized in cross-coupling reactions such a

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active pyridine derivatives. Its stereochemistry makes it valuable for asymmetric synthesis, where it helps introduce specific chirality into target molecules. Commonly employed in the preparation of neuroactive compounds and enzyme inhibitors due to the reactivity of the bromo group and the structural influence of the methoxyethyl side chain. Also utilized in cross-coupling reactions such as Suzuki or Negishi couplings to build complex heterocyclic systems in medicinal chemistry research.

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