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1,2-Dimethyl-5-hydroxyindole-3-Carboxylate Ethyl

Category:

Other Intermediates

CAS NO:

15574-49-9

Standard:

In-house Standards,

Price Range:

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Main Sales Markets:

North America,Central/South America,Western Europe,Eastern Europe,Australasia,Asia,Middle East,Africa

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Jinan Xinnuo Pharmaceutical Co., Ltd

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Basic Info

CAS Number

15574-49-9

Pharmacopoeia

In-house Standards

Grade

Pharmaceutical Grade

Is Manufacturer

YES

Samples Provided

Product Description

Cigna Qingdao is mainly engaged in the intermediates of febuxostatin, ceflothrin, eprazole, flubiprofen, phenalidone, tovaptan, rivaroxaban and Avanafil, terbinafine intermediates, thioacetamide and thiophene and their derivatives.

AI Product Description

*The following content is generated by AI and is for reference only.

1,2-Dimethyl-5-hydroxyindole-3-carboxylate ethyl is a specialized organic compound belonging to the indole family, widely utilized in advanced chemical synthesis and pharmaceutical research. Its molecular formula is C₁₃H₁₅NO₃, reflecting a complex structure composed of thirteen carbon atoms, fifteen hydrogen atoms, one nitrogen atom, and three oxygen atoms. While specific CAS registry numbers for this exact derivative may vary depending on precise stereochemistry or salt forms, it generally falls under the broader classification of substituted indole esters used as key intermediates. This molecule features a hydroxy group at the fifth position and an ethyl carboxylate moiety at the third position, flanked by methyl groups on the nitrogen and adjacent carbon, which significantly influences its electronic properties and reactivity profile. The primary application of 1,2-dimethyl-5-hydroxyindole-3-carboxylate ethyl lies in the development of novel bioactive compounds, particularly within the field of medicinal chemistry. Researchers frequently employ such substituted indoles as building blocks for synthesizing potential anticancer agents, anti-inflammatory drugs, and neuroprotective molecules. The presence of the hydroxyl group allows for further functionalization through etherification or esterification reactions, while the ester group provides a versatile handle for hydrolysis or transesterification to generate diverse derivatives. In materials science, similar indole structures are investigated for their potential use in organic electronics due to their conjugated pi-systems, although this specific derivative is predominantly valued for its pharmacological precursors. Synthesis of this compound typically involves multi-step organic pathways, often starting from dimethyltryptophan derivatives or utilizing Fischer indole synthesis protocols followed by selective esterification. High-purity samples are essential for reliable experimental results in drug discovery pipelines. Due to its sensitivity to oxidation and light, proper storage conditions involving inert atmospheres and low temperatures are recommended to maintain stability. As a niche chemical intermediate, it serves as a critical tool for academic laboratories and industrial R&D departments aiming to expand the chemical space of indole-based therapeutics. Continuous monitoring of regulatory compliance regarding hazardous substances is necessary when handling this material in large-scale production environments. Ultimately, this compound represents a sophisticated bridge between basic organic synthesis and applied pharmaceutical innovation, offering unique structural advantages for creating next-generation therapeutic candidates with improved efficacy and selectivity profiles.