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2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)-3-methylbutanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

148991-43-9

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148991-43-9 Usage

Derivative of pyrrole

The compound is based on a pyrrole ring, which is a five-membered ring with four carbon atoms and one nitrogen atom.

Contains a carboxylic acid functional group

The compound has a carboxylic acid group (-COOH) attached to a carbon chain, which gives it acidic properties.

Used as an intermediate in the synthesis of pharmaceuticals and organic compounds

The compound is commonly used as a building block in the production of more complex molecules in the pharmaceutical and organic chemistry industries.

Potential to exhibit biological activities

The compound's structural features make it a promising candidate for medicinal chemistry research, as it may have therapeutic effects.

Important target for medicinal chemistry research

The compound's potential biological activities and unique structure make it a valuable subject for further study in the field of medicinal chemistry.

Applications in the field of organic synthesis

The compound may be used in the production of other valuable chemical compounds through organic synthesis processes.

Check Digit Verification of cas no

The CAS Registry Mumber 148991-43-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,9,9 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 148991-43:
(8*1)+(7*4)+(6*8)+(5*9)+(4*9)+(3*1)+(2*4)+(1*3)=179
179 % 10 = 9
So 148991-43-9 is a valid CAS Registry Number.

148991-43-9Downstream Products

148991-43-9Relevant articles and documents

L-valine-substituted maleimide derivative as well as preparation method and application thereof

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Paragraph 0040; 0046, (2018/11/03)

The invention discloses an L-valine-substituted maleimide derivative as well as a preparation method thereof. The preparation method comprises the following steps: synthesizing 1-aryl-3-methyl-4-formyl-5-(1,2,4-triazolyl)pyrazol; then adopting a method of

D-valine substituted maleimide derivative, and preparation method and application thereof

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Paragraph 0040; 0046, (2018/11/22)

The invention discloses a D-valine substituted maleimide derivative and a preparation method thereof. The preparation method comprises compositing 1-aryl-3-methyl-4-formyl-5-(1,2,4-triazolyl)pyrazol;subjecting the 1-aryl-3-methyl-4-formyl-5-(1,2,4-triazol

Design and synthesis of a novel DNA-encoded chemical library using Diels-Alder cycloadditions

Buller, Fabian,Mannocci, Luca,Zhang, Yixin,Dumelin, Christoph E.,Scheuermann, Joerg,Neri, Dario

supporting information; experimental part, p. 5926 - 5931 (2009/05/31)

DNA-encoded chemical libraries are increasingly being employed for the identification of binding molecules to protein targets of pharmaceutical relevance. Here, we describe the synthesis and characterization of a DNA-encoded chemical library, consisting of 4000 compounds generated by Diels-Alder cycloaddition reactions. The compounds were encoded with unique DNA fragments which were generated through a stepwise assembly process and serve as amplifiable bar codes for the identification and relative quantification of library members.

Synthesis and properties of chiral N,N-maleoyl derivatives and Diels-Alder reactions with cyclopentadiene

Bodtke,Otto, Hans-Hartwig

, p. 803 - 813 (2007/10/03)

Maleyl amino acid derivatives were prepared from maleic anhydride and cyclized by reaction with ZnCl2 and hexamethyldisilazane yielding maleoyl derivatives. These derivatives were used as dienophiles in cycloadditions with cyclopentadiene. The

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