Ethyl 2-bromo-2-(o-tolyl)acetate

95%

Reagent Code: #180720
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CAS Number 37051-41-5

science Other reagents with same CAS 37051-41-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.12 g/mol
Formula C₁₁H₁₃BrO₂
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block for α-substituted carbonyl compounds due to the presence of both ester and bromo functional groups, enabling transformations such as nucleophilic substitution and cyclization reactions. Commonly employed in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules where the o-tolyl group contributes to steric and electronic properties. Its reactivity allows for easy introduction into heterocyclic systems, making it valuable in medicinal chemistry research and development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,770.00
inventory 250mg
10-20 days ฿25,110.00
inventory 1g
10-20 days ฿67,760.00

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Ethyl 2-bromo-2-(o-tolyl)acetate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block for α-substituted carbonyl compounds due to the presence of both ester and bromo functional groups, enabling transformations such as nucleophilic substitution and cyclization reactions. Commonly employed in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules where the o-tolyl group contributes to steric and electronic p

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block for α-substituted carbonyl compounds due to the presence of both ester and bromo functional groups, enabling transformations such as nucleophilic substitution and cyclization reactions. Commonly employed in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules where the o-tolyl group contributes to steric and electronic properties. Its reactivity allows for easy introduction into heterocyclic systems, making it valuable in medicinal chemistry research and development.

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