(R)-2-(1,3-dioxoisoindolin-2-yl)propanoic acid

95%

Reagent Code: #232284
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CAS Number 29588-83-8

science Other reagents with same CAS 29588-83-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.19 g/mol
Formula C₁₁H₉NO₄
badge Registry Numbers
MDL Number MFCD24479562
inventory_2 Storage & Handling
Storage 2-8°C, Sealed

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of biologically active compounds where stereochemistry plays a critical role. Its structure allows for the introduction of a carboxylic acid functionality in conjunction with a rigid, aromatic imide group, making it valuable in asymmetric synthesis and medicinal chemistry. Commonly employed in the development of enantiomerically pure drugs, including certain protease inhibitors and targeted cancer therapies. Also utilized in the preparation of peptide mimetics and as a building block in the design of small molecule therapeutics with improved metabolic stability and binding selectivity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿3,410.00
1g
10-20 days ฿9,620.00
5g
10-20 days ฿39,290.00
(R)-2-(1,3-dioxoisoindolin-2-yl)propanoic acid
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of biologically active compounds where stereochemistry plays a critical role. Its structure allows for the introduction of a carboxylic acid functionality in conjunction with a rigid, aromatic imide group, making it valuable in asymmetric synthesis and medicinal chemistry. Commonly employed in the development of enantiomerically pure drugs, including certain protease inhibitors and targeted cancer therapies.

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of biologically active compounds where stereochemistry plays a critical role. Its structure allows for the introduction of a carboxylic acid functionality in conjunction with a rigid, aromatic imide group, making it valuable in asymmetric synthesis and medicinal chemistry. Commonly employed in the development of enantiomerically pure drugs, including certain protease inhibitors and targeted cancer therapies. Also utilized in the preparation of peptide mimetics and as a building block in the design of small molecule therapeutics with improved metabolic stability and binding selectivity.

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