10577-14-7

Basic information

• Product Name: 2-[2-Chloro-1-[(dimethoxyphosphinothioyl)thio]ethyl]-2H-isoindole-1,3-dione
• Synonyms: 2-[2-Chloro-1-[(dimethoxyphosphinothioyl)thio]ethyl]-2H-isoindole-1,3-dione;ENT-27321;Hercules-14504;Ai3-27321;Brn 1548688;Nsc 190921;Phosphorodithioic acid, o,o-dimethyl ester, S-ester with N-(2-chloro-1- mercaptoethyl)phthalimide;Phosphorodithioic acid, S-(2-chloro-1-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)ethyl) o,o-dimethyl ester
• CAS NO: 10577-14-7
• Molecular Formula: C12H13 Cl N O4 P S2
• Molecular Weight: 0
• Mol File: 10577-14-7.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 447.6°C at 760 mmHg
• Flash Point: 224.5°C
• Appearance: /
• Density: 1.515g/cm³
• Vapor Pressure: 3.31E-08mmHg at 25°C
• Refractive Index: 1.637
• CAS DataBase Reference: 2-[2-Chloro-1-[(dimethoxyphosphinothioyl)thio]ethyl]-2H-isoindole-1,3-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[2-Chloro-1-[(dimethoxyphosphinothioyl)thio]ethyl]-2H-isoindole-1,3-dione(10577-14-7)
• EPA Substance Registry System: 2-[2-Chloro-1-[(dimethoxyphosphinothioyl)thio]ethyl]-2H-isoindole-1,3-dione(10577-14-7)

Safety Data

• Hazardous Substances Data: 10577-14-7(Hazardous Substances Data)

Usage

Derivative of isoindole-1,3-dione

A modified version of the isoindole-1,3-dione core structure, which is a heterocyclic aromatic compound.

Phosphinothioylthio group

A phosphorus-sulfur-thioether functional group present in the compound, which may contribute to its biological activity and reactivity.

Potential inhibitor of acetylcholinesterase

The compound may interfere with the activity of acetylcholinesterase, an enzyme responsible for breaking down the neurotransmitter acetylcholine in the brain.

Increased acetylcholine levels

Inhibition of acetylcholinesterase may lead to higher levels of acetylcholine, which could have therapeutic implications for neurodegenerative diseases.

Potential target for Alzheimer's treatment

The compound's ability to modulate acetylcholine levels in the brain makes it a candidate for further research in the treatment of Alzheimer's disease and other neurodegenerative disorders.

Presence of chloro and dimethoxy substituents

These functional groups may confer additional pharmacological properties or reactivity to the compound, influencing its potential therapeutic applications.

Unique structure and biological activity

The compound's distinct chemical structure and potential biological effects make it an interesting subject for further study in medicinal chemistry.

InChI:InChI=1/C12H13ClNO4PS2/c1-17-19(20,18-2)21-7-10(13)14-11(15)8-5-3-4-6-9(8)12(14)16/h3-6,10H,7H2,1-2H3

Relevant articles and documents

An image forming device

PROBLEM TO BE SOLVED: To improve work efficiency for attaching and detaching a process unit in which a photoreceptor drum and an intermediate transfer belt are unitized to and from a printer body by reducing load on an operator when attaching and detaching the process unit to and from the printer body. SOLUTION: The process unit 30 is constituted by unitizing the photoreceptor 2, the intermediate transfer belt 6, an electrifying roll 3 and a cleaning device 20, etc.. Rails 56 and 58 on which projecting parts 36 and 38 provided on both ends of the process unit 30 can be slid are formed on a supporting member 60 of a main body cover 52. By opening the body cover 52 toward the front direction (direction of an arrow A) of the printer body 50, the process unit 30 is moved from a first position T1to a second position T2. Then, by pulling out the process unit 30 in a direction diagonally upward in front along the rails 56 and 58 from the second position T2, the process unit 30 is extracted. COPYRIGHT: (C)2006,JPOandNCIPI