2983-42-8

Basic information

• Product Name: 1-Penten-3-one, 5-(4-morpholinyl)-1-phenyl-, hydrochloride
• CAS NO: 2983-42-8
• Molecular Formula: C15H19NO2.ClH
• Molecular Weight: 281.782
• Mol File: 2983-42-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-Penten-3-one, 5-(4-morpholinyl)-1-phenyl-, hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Penten-3-one, 5-(4-morpholinyl)-1-phenyl-, hydrochloride(2983-42-8)
• EPA Substance Registry System: 1-Penten-3-one, 5-(4-morpholinyl)-1-phenyl-, hydrochloride(2983-42-8)

Safety Data

• Hazardous Substances Data: 2983-42-8(Hazardous Substances Data)

Usage

Type of compound

Chemical compound

Uses

Production of pharmaceuticals and agrochemicals, potential use as a building block in organic synthesis, research purposes

Properties

Stability and solubility in aqueous solutions

Other notes

Versatile chemical with a range of applications in the chemical industry.

Upstream product

• 110-91-8 morpholine 
• 50-00-0 formaldehyd 
• 1896-62-4 (E)-benzalacetone 
• 5625-90-1 4-(morpholinomethyl)morpholine 
• 52853-19-7 N-(methylene)morpholinium chloride 
• 122-57-6 1-Phenylbut-1-en-3-one 

Downstream Products

• 73291-51-7 1-phenyl-1,4-pentadien-3-one 
• 1374446-66-8 (E)-5-(morpholin-4-yl)-1-phenylpent-1-en-3-one thiosemicarbazone hydrochloride 
• 132105-82-9 5-morpholino-1t-phenyl-pent-1-en-3-one-phenylhydrazone; hydrochloride 

Relevant articles and documents

An efficient water-mediated synthetic route for the alkylation of heteroarenes

An efficient synthetic route has been described for the alkylation of 1H-indole, 1H-benzimidazole, and 1H-benzotriazole. This approach features the alkylation of heteroaromatics through in situ generated enones from ketonic Mannich bases under metal-free conditions. A series of alkylated heteroaromatics have been synthesized via the K10 catalyzed alkylation reactions of these heteroaromatics with a variety of ketonic Mannich bases. Environmentally benign K10 catalyst, water-mediated mild reaction conditions, and the efficient synthesis of alkylated products are the advantages of this alkylation method.

Intramolecular cyclization and cytotoxicities of some Mannich bases of styryl ketones

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Mannich Bases of 4-Phenyl-3-buten-2-one: A New Class of Antiherpes Agent

The morpholine Mannich base of 4-phenyl-3-buten-2-one was found to have activity in model infections of herpes simplex.The activity was essentially equivalent to that of disodium phosphonoacetate.This paper presents the biological activity and synthesis o