89516-34-7

Basic information

• Product Name: 1-(10-{N-[2-(4-chlorophenyl)-1,1-dimethylethyl]glycyl}-10H-phenothiazin-2-yl)ethanone
• CAS NO: 89516-34-7
• Molecular Formula: C₂₆H₂₅ClN₂O₂S
• Molecular Weight: 465.0069
• Mol File: 89516-34-7.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 691.3°C at 760 mmHg
• Flash Point: 371.9°C
• Density: 1.267g/cm³
• Vapor Pressure: 5.81E-19mmHg at 25°C
• Refractive Index: 1.636
• CAS DataBase Reference: 1-(10-{N-[2-(4-chlorophenyl)-1,1-dimethylethyl]glycyl}-10H-phenothiazin-2-yl)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(10-{N-[2-(4-chlorophenyl)-1,1-dimethylethyl]glycyl}-10H-phenothiazin-2-yl)ethanone(89516-34-7)
• EPA Substance Registry System: 1-(10-{N-[2-(4-chlorophenyl)-1,1-dimethylethyl]glycyl}-10H-phenothiazin-2-yl)ethanone(89516-34-7)

Safety Data

• Hazardous Substances Data: 89516-34-7(Hazardous Substances Data)

Usage

Chemical class

Derivative of phenothiazine

Explanation

Phenothiazine is a chemical compound commonly used in the pharmaceutical industry to synthesize antipsychotic drugs.

Explanation

The core structure of the compound is based on the phenothiazine ring system.

Explanation

The compound contains a glycine residue, which is an amino acid, attached to the phenothiazine core structure.

Explanation

The compound has a 4-chlorophenyl group, which is a phenyl ring with a chlorine atom at the 4th position.

Explanation

The compound also contains a 1,1-dimethylethyl group, which is a branched alkyl group with two methyl groups attached to a central carbon atom.

Explanation

The presence of an ethanone (ketones) functional group adds to the complexity of the molecule and may influence its chemical properties.

Explanation

Due to its complex structure, the compound may exhibit a range of pharmacological properties, making it suitable for various medical and experimental purposes.

Explanation

The compound's unique structure and properties could make it useful in the development of new drugs or for research purposes in the pharmaceutical industry.

Core structure

10H-phenothiazin-2-yl

Modification

Glycine residue attachment

Substituent

4-chlorophenyl group

Substituent

1,1-dimethylethyl group

Functional group

Ethanone moiety

Pharmacological properties

Potential range of properties

Potential applications

Medical and experimental uses

Upstream product

• 461-78-9 Chlorphentermine 
• 80838-42-2 2-acetyl-10-(chloroacetyl)-10H-phenothiazine 

Relevant articles and documents

Phenothiazine Derivatives as Antiparkinsonian Agents

2-Acetyl-10-chloroacetylphenothiazine (II) undergoes condensation with substituted amines to yield 2-acetyl-10-(arylalkylaminoacetyl)phenothiazines (III).Mannich reaction of 2-acetylphenothiazine (I) with amines gives 2-(N'-substituted-propanoyl)phenothia