39198-78-2

Basic information

• Product Name: 4-CYCLOPENTYL-MORPHOLINE
• Synonyms: 4-CYCLOPENTYL-MORPHOLINE;Morpholine, 4-cyclopentyl- (7CI,9CI)
• CAS NO: 39198-78-2
• Molecular Formula: C₉H₁₇NO
• Molecular Weight: 155.23738
• Product Categories: CYCLOPENTANE
• Mol File: 39198-78-2.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 217.953 °C at 760 mmHg
• Flash Point: 62.628 °C
• Appearance: /
• Density: 1.029 g/cm³
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4-CYCLOPENTYL-MORPHOLINE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-CYCLOPENTYL-MORPHOLINE(39198-78-2)
• EPA Substance Registry System: 4-CYCLOPENTYL-MORPHOLINE(39198-78-2)

Safety Data

• Hazardous Substances Data: 39198-78-2(Hazardous Substances Data)

Usage

General Description

4-Cyclopentyl-Morpholine, also known as CPMO, is a versatile organic chemical compound that predominantly belongs to the group of Morpholines. Its systematic name is 4-Cyclopentylmorpholine. 4-CYCLOPENTYL-MORPHOLINE is particularly important in pharmaceutical and chemical research, as it serves as a building block in the synthesis of various drugs. Known for its physical state of liquid at Normal Room Temperature, it does not have any color of its own. Thus, 4-Cyclopentylmorpholine is recognised as its chemical stability, reactive nature, high purity level, and precise pH value.

Upstream product

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Relevant articles and documents

Colloid and nanosized catalysts in organic synthesis: IX hydrogenation of enamines with hydrogen at atmospheric pressure

Hydrogenation of enamines with hydrogen at atmospheric pressure was performed using nickel nanoparticles as a catalyst. The reaction may be used to produce tertiary amines under mild conditions using an accessible catalyst.

Trichloroacetylhydrazones: New highly reactive alkylating agents

The behavior of trichloroacylhydrazones as new highly reactive alkylating agents is disclosed; various secondary amines are alkylated within a few minutes at room temperature, and similar alkylating reductions were found with malonates.

1,3-CYCLOADDITIONS OF A THIONITROSO S-SULFIDE

The thionitroso S-sulfide 5 adds to (E)-cyclooctene, (E,Z)-1,5-cyclooctadiene, and norbornene to give 1,2,3-dithiazolidines, whereas enamines undergo electrophilic substitution.