873064-07-4

Basic information

• Product Name: 1-Piperidinecarboxylic acid, 4-hydroxy-, 1-[(3R,5R)-4-[(4-chlorophenyl)sulfonyl]-5-propyl-3-morpholinyl]cycloprop yl ester
• CAS NO: 873064-07-4
• Molecular Formula: C22H31ClN2O6S
• Mol File: 873064-07-4.mol
• Article Data: 0

Chemical Properties

• CAS DataBase Reference: 1-Piperidinecarboxylic acid, 4-hydroxy-, 1-[(3R,5R)-4-[(4-chlorophenyl)sulfonyl]-5-propyl-3-morpholinyl]cycloprop yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Piperidinecarboxylic acid, 4-hydroxy-, 1-[(3R,5R)-4-[(4-chlorophenyl)sulfonyl]-5-propyl-3-morpholinyl]cycloprop yl ester(873064-07-4)
• EPA Substance Registry System: 1-Piperidinecarboxylic acid, 4-hydroxy-, 1-[(3R,5R)-4-[(4-chlorophenyl)sulfonyl]-5-propyl-3-morpholinyl]cycloprop yl ester(873064-07-4)

Safety Data

• Hazardous Substances Data: 873064-07-4(Hazardous Substances Data)

Usage

Molecular structure

The compound consists of a piperidine ring, a cyclopropane ring, a 4-hydroxy group, a sulfonyl group, a chlorophenyl moiety, a propyl group, and a morpholinyl group.

Functional groups

The compound contains several functional groups, including a carboxylic acid, a hydroxyl group, a sulfonyl group, and an ester group.

Stereochemistry

The compound has two chiral centers at the 3rd and 5th positions of the cyclopropane ring, with R configurations.

Substitution pattern

The compound has a substituted pattern with a chlorophenyl group attached to the sulfonyl group, a propyl group attached to the morpholinyl group, and an ester linkage between the cyclopropane and piperidine rings.

Physical properties

The compound is likely to be a solid with a high melting point due to the presence of multiple intermolecular forces, such as hydrogen bonding and van der Waals forces.

Solubility

The compound may exhibit low solubility in water due to the presence of the hydrophobic cyclopropane and morpholinyl groups.

Reactivity

The compound may undergo various chemical reactions, such as nucleophilic substitution, due to the presence of the ester group and the electron-deficient chlorophenyl group.

Biological activity

The compound has potential pharmaceutical and biological activities, which would depend on its detailed structure and reactivity.

Synthesis

The compound can be synthesized through a series of chemical reactions, including the formation of the piperidine ring, the cyclopropane ring, and the ester linkage.

Applications

The compound may have potential applications in the pharmaceutical industry as a drug candidate or as an intermediate in the synthesis of other biologically active compounds.