Welcome to LookChem.com Sign In|Join Free
  • or
2-(cyclohepta-2,4,6-trien-1-yl)-1H-isoindole-1,3(2H)-dione is a unique chemical compound that belongs to the class of isoindole-1,3-diones. It features a cyclohepta-2,4,6-trien-1-yl group attached to the 2-position of an isoindole ring, which incorporates a 1,3-dione functional group. 2-(cyclohepta-2,4,6-trien-1-yl)-1H-isoindole-1,3(2H)-dione is known for its distinctive molecular structure and reactivity, which positions it as a promising candidate for various applications in the realms of organic synthesis, medicinal chemistry, and material science. The exploration of its properties and potential uses is an active area of research within the chemical and pharmaceutical sciences.

92497-80-8

Post Buying Request

92497-80-8 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

92497-80-8 Usage

Uses

Used in Organic Synthesis:
2-(cyclohepta-2,4,6-trien-1-yl)-1H-isoindole-1,3(2H)-dione is utilized as a key intermediate in organic synthesis for the creation of complex organic molecules. Its unique structure allows for versatile chemical reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-(cyclohepta-2,4,6-trien-1-yl)-1H-isoindole-1,3(2H)-dione is employed as a building block for the development of novel therapeutic agents. Its reactivity and structural features enable the design of new compounds with potential biological activities, targeting a range of diseases and medical conditions.
Used in Material Science:
2-(cyclohepta-2,4,6-trien-1-yl)-1H-isoindole-1,3(2H)-dione also finds applications in material science, where it is used to develop new materials with specific properties. Its incorporation into polymers, for instance, can lead to materials with enhanced mechanical, thermal, or electrical characteristics, depending on the desired application.
Used in Pharmaceutical Research:
In pharmaceutical research, 2-(cyclohepta-2,4,6-trien-1-yl)-1H-isoindole-1,3(2H)-dione is explored for its potential as a lead compound in drug discovery. Its unique chemical properties may contribute to the development of new drugs with improved efficacy, selectivity, and safety profiles for the treatment of various diseases.
Used in Chemical Research:
2-(cyclohepta-2,4,6-trien-1-yl)-1H-isoindole-1,3(2H)-dione serves as a subject of interest in chemical research, where its properties, reactivity, and potential applications are being investigated. This research aims to uncover new insights into its behavior and to expand the understanding of its role in chemical reactions and processes.

Check Digit Verification of cas no

The CAS Registry Mumber 92497-80-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,4,9 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92497-80:
(7*9)+(6*2)+(5*4)+(4*9)+(3*7)+(2*8)+(1*0)=168
168 % 10 = 8
So 92497-80-8 is a valid CAS Registry Number.

92497-80-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-cyclohepta-2,4,6-trien-1-ylisoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names 7-phthalimido-1,3,5-cycloheptatriene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:92497-80-8 SDS

92497-80-8Relevant academic research and scientific papers

C–N Coupling of Azoles or Imides with Carbocations Generated by Electrochemical Oxidation

Shao, Xiaoqing,Tian, Lifang,Wang, Yahui

supporting information, p. 4089 - 4094 (2019/06/25)

An approach for electrochemistry-enabled intermolecular oxidative C–N coupling reactions of azoles and imides with 1,3,5-cycloheptatriene and xanthenes is disclosed. The reaction proceeds via the anodic oxidation of 1,3,5-cycloheptatriene or xanthenes to

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 92497-80-8