Methyl2-(4-ethynylphenyl)acetate

98%

Reagent Code: #213655
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CAS Number 154498-13-2

science Other reagents with same CAS 154498-13-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.20 g/mol
Formula C₁₁H₁₀O₂
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MDL Number MFCD13194554
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Its ethynyl group allows participation in coupling reactions, such as Sonogashira or click chemistry, making it valuable in drug discovery and development of bioactive molecules. The ester functionality can be hydrolyzed or transformed to introduce carboxylic acid derivatives, enabling further structural modifications. Commonly employed in the preparation of conjugated systems for materials science and in the synthesis of analogs for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,510.00
inventory 250mg
10-20 days ฿10,840.00
inventory 1g
10-20 days ฿28,410.00
Methyl2-(4-ethynylphenyl)acetate
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Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Its ethynyl group allows participation in coupling reactions, such as Sonogashira or click chemistry, making it valuable in drug discovery and development of bioactive molecules. The ester functionality can be hydrolyzed or transformed to introduce carboxylic acid derivatives, enabling further structural modifications. Commonly employed in the preparation of conjugated systems for materials science and in the synthesis o

Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Its ethynyl group allows participation in coupling reactions, such as Sonogashira or click chemistry, making it valuable in drug discovery and development of bioactive molecules. The ester functionality can be hydrolyzed or transformed to introduce carboxylic acid derivatives, enabling further structural modifications. Commonly employed in the preparation of conjugated systems for materials science and in the synthesis of analogs for structure-activity relationship studies.

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