280110-66-9

Basic information

• Product Name: 1-Piperidinecarboxylic acid, 4-(5-methyl-1,2,4-oxadiazol-3-yl)-, 1,1-dimethylethyl ester
• Synonyms: 1-Piperidinecarboxylic acid, 4-(5-methyl-1,2,4-oxadiazol-3-yl)-, 1,1-dimethylethyl ester;tert-butyl 4-(5-methyl-1,2,4-oxadiazol-3-yl)piperidine-1-carboxylate
• CAS NO: 280110-66-9
• Molecular Formula: C13H21N3O3
• Molecular Weight: 267.32414
• Mol File: 280110-66-9.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-Piperidinecarboxylic acid, 4-(5-methyl-1,2,4-oxadiazol-3-yl)-, 1,1-dimethylethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Piperidinecarboxylic acid, 4-(5-methyl-1,2,4-oxadiazol-3-yl)-, 1,1-dimethylethyl ester(280110-66-9)
• EPA Substance Registry System: 1-Piperidinecarboxylic acid, 4-(5-methyl-1,2,4-oxadiazol-3-yl)-, 1,1-dimethylethyl ester(280110-66-9)

Safety Data

• Hazardous Substances Data: 280110-66-9(Hazardous Substances Data)

Usage

Chemical Class

Piperidinecarboxylic acids

Explanation

This compound belongs to a class of organic compounds that includes piperidine, a five-membered nitrogen-containing heterocyclic ring, and a carboxyl group (-COOH).

Explanation

It is commonly used in the synthesis of various pharmaceuticals and agrochemicals due to its reactive functional groups and ability to form new compounds easily.

Explanation

The presence of this ester group improves the compound's solubility and stability, making it suitable for a wide range of applications.

Explanation

This group enhances the biological activity of the compound, which can potentially be used in the development of new drugs or pesticides.

Explanation

Due to its unique chemical structure and properties, this compound has applications in the fields of medicine (e.g., drug development) and agriculture (e.g., pesticide development).

Explanation

The compound's functional groups, such as the carboxyl and ester groups, make it reactive and capable of undergoing various chemical reactions, such as esterification, amidation, and substitution reactions.

Explanation

The compound consists of a piperidine ring with a carboxyl group attached to position 1, an ester group (1,1-dimethylethyl) at position 1, and a 5-methyl-1,2,4-oxadiazol-3-yl group at position 4.

Explanation

The compound's unique structure and biological activity make it a promising candidate for the development of new drugs, particularly in the areas of central nervous system disorders, pain management, and anti-inflammatory treatments.

Explanation

The 5-methyl-1,2,4-oxadiazol-3-yl group in the compound may contribute to its pesticidal properties, making it a potential candidate for the development of new pesticides for agricultural use.

Explanation

The presence of the 1,1-dimethylethyl ester group increases the compound's solubility in organic solvents, which is beneficial for its use in chemical synthesis and formulation processes.

Upstream product

• 280110-63-6 4-(N-hydroxycarbamimidoyl)piperidine-1-carboxylic acid tert-butyl ester 
• 75-05-8 acetonitrile 
• 108-24-7 acetic anhydride 
• 1421065-40-8 4-(N-hydroxycarbamimidoyl)piperidine-1-carboxylic acid tert-butyl ester 
• 1421065-40-8 (E)-tert-butyl 4-(N’-hydroxycarbamimidoyl)piperidine-1-carboxylate 
• 64-19-7 acetic acid 
• 91419-52-2 1-tert-butoxycarbonyl-4-cyanopiperidine 

Downstream Products

• 757175-70-5 5-methyl-3-(piperidin-4-yl)-1,2,4-oxadiazole 

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