Butanedioic acid, 1-(1,1-dimethylethyl) 4-(2,5-dioxo-1-pyrrolidinyl) ester

≥95%

Reagent Code: #151285
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CAS Number 138833-93-9

science Other reagents with same CAS 138833-93-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.27 g/mol
Formula C₁₂H₁₇NO₆
badge Registry Numbers
MDL Number MFCD30290246
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in peptide coupling and polymer chemistry. Its activated ester functionality allows efficient amide bond formation, making it valuable in pharmaceutical manufacturing and bioconjugation processes. The tert-butyl group provides steric protection, enabling selective reactions in multi-step syntheses. Commonly employed in the production of specialty polymers and drug delivery systems where controlled reactivity and stability are required.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,920.00
250mg
10-20 days ฿3,200.00
500mg
10-20 days ฿5,280.00
1g
10-20 days ฿8,000.00
5g
10-20 days ฿24,000.00
10g
10-20 days ฿40,000.00
25g
10-20 days ฿80,000.00
Butanedioic acid, 1-(1,1-dimethylethyl) 4-(2,5-dioxo-1-pyrrolidinyl) ester
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Used as an intermediate in organic synthesis, particularly in peptide coupling and polymer chemistry. Its activated ester functionality allows efficient amide bond formation, making it valuable in pharmaceutical manufacturing and bioconjugation processes. The tert-butyl group provides steric protection, enabling selective reactions in multi-step syntheses. Commonly employed in the production of specialty polymers and drug delivery systems where controlled reactivity and stability are required.

Used as an intermediate in organic synthesis, particularly in peptide coupling and polymer chemistry. Its activated ester functionality allows efficient amide bond formation, making it valuable in pharmaceutical manufacturing and bioconjugation processes. The tert-butyl group provides steric protection, enabling selective reactions in multi-step syntheses. Commonly employed in the production of specialty polymers and drug delivery systems where controlled reactivity and stability are required.

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