(E)-2-Cyano-4,4-dimethylpent-2-enoic acid

98%

Reagent Code: #180705
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CAS Number 39168-28-0

science Other reagents with same CAS 39168-28-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.18 g/mol
Formula C₈H₁₁NO₂
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its conjugated nitrile and carboxylic acid functionalities make it suitable for carbon-chain extension reactions and cyclization processes. Commonly employed in the development of α,β-unsaturated carbonyl systems, it participates in Michael additions and Diels-Alder reactions. Also utilized in the synthesis of specialty monomers for functional polymers due to its reactive double bond and polar groups.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿3,500.00
250mg
10-20 days ฿5,900.00
1g
10-20 days ฿18,700.00
(E)-2-Cyano-4,4-dimethylpent-2-enoic acid
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its conjugated nitrile and carboxylic acid functionalities make it suitable for carbon-chain extension reactions and cyclization processes. Commonly employed in the development of α,β-unsaturated carbonyl systems, it participates in Michael additions and Diels-Alder reactions. Also utilized in the synthesis of specialty monomers for functional polymers due to its reactive double bond and po

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its conjugated nitrile and carboxylic acid functionalities make it suitable for carbon-chain extension reactions and cyclization processes. Commonly employed in the development of α,β-unsaturated carbonyl systems, it participates in Michael additions and Diels-Alder reactions. Also utilized in the synthesis of specialty monomers for functional polymers due to its reactive double bond and polar groups.

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