tert.-Butyl methyl malonate

≥97%

Reagent Code: #144531
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CAS Number 42726-73-8

science Other reagents with same CAS 42726-73-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.19 g/mol
Formula C₈H₁₄O₄
badge Registry Numbers
MDL Number MFCD00042856
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used primarily as a building block in organic synthesis, particularly in the pharmaceutical and agrochemical industries. Its ester groups allow for selective hydrolysis and decarboxylation, making it valuable in the preparation of carboxylic acids and ketones. Commonly employed in the synthesis of active pharmaceutical ingredients (APIs) where it serves as a precursor for introducing branched alkyl chains. Also utilized in the production of specialty polymers and fragrances due to its stability and reactivity profile. Its tert-butyl group provides steric hindrance, which can help control reaction selectivity in complex multi-step syntheses.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿143.00
inventory 5g
10-20 days ฿520.00
inventory 25g
10-20 days ฿1,890.00

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tert.-Butyl methyl malonate
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Used primarily as a building block in organic synthesis, particularly in the pharmaceutical and agrochemical industries. Its ester groups allow for selective hydrolysis and decarboxylation, making it valuable in the preparation of carboxylic acids and ketones. Commonly employed in the synthesis of active pharmaceutical ingredients (APIs) where it serves as a precursor for introducing branched alkyl chains. Also utilized in the production of specialty polymers and fragrances due to its stability and react

Used primarily as a building block in organic synthesis, particularly in the pharmaceutical and agrochemical industries. Its ester groups allow for selective hydrolysis and decarboxylation, making it valuable in the preparation of carboxylic acids and ketones. Commonly employed in the synthesis of active pharmaceutical ingredients (APIs) where it serves as a precursor for introducing branched alkyl chains. Also utilized in the production of specialty polymers and fragrances due to its stability and reactivity profile. Its tert-butyl group provides steric hindrance, which can help control reaction selectivity in complex multi-step syntheses.

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