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
• Article Data: 5

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

Different sources of media describe the Explanation of 280110-66-9 differently. You can refer to the following data:
1. This compound belongs to a class of organic compounds that includes piperidine, a five-membered nitrogen-containing heterocyclic ring, and a carboxyl group (-COOH).
2. 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.
3. The presence of this ester group improves the compound's solubility and stability, making it suitable for a wide range of applications.
4. This group enhances the biological activity of the compound, which can potentially be used in the development of new drugs or pesticides.
5. 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).
6. 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.
7. 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.
8. 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.
9. 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.
10. 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 
• 1421065-40-8 4-(N-hydroxycarbamimidoyl)piperidine-1-carboxylic acid tert-butyl ester 
• 108-24-7 acetic anhydride 
• 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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