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(5,6-DICHLORO-1,3-DIOXO-1,3-DIHYDRO-ISOINDOL-2-YL)-ACETIC ACID, also known as Isoindol-2-ylacetic acid, is a chemical compound that belongs to the class of organic compounds known as phenoxyacetic acid derivatives. It is widely used in the pharmaceutical industry for the synthesis of various drugs. (5,6-DICHLORO-1,3-DIOXO-1,3-DIHYDRO-ISOINDOL-2-YL)-ACETIC ACID has the potential to act as an immunosuppressive and anti-inflammatory agent, making it a promising candidate for the treatment of autoimmune diseases and conditions characterized by abnormal immune responses. Additionally, it is being studied for its potential use in the treatment of cardiovascular diseases and cancer, highlighting its importance in drug development and medical research.

111104-25-7

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111104-25-7 Usage

Uses

Used in Pharmaceutical Industry:
(5,6-DICHLORO-1,3-DIOXO-1,3-DIHYDRO-ISOINDOL-2-YL)-ACETIC ACID is used as a key intermediate in the synthesis of various drugs, contributing to the development of new therapeutic agents.
Used in Autoimmune Disease Treatment:
(5,6-DICHLORO-1,3-DIOXO-1,3-DIHYDRO-ISOINDOL-2-YL)-ACETIC ACID is used as an immunosuppressive and anti-inflammatory agent for the treatment of autoimmune diseases, helping to regulate abnormal immune responses and alleviate symptoms.
Used in Cardiovascular Disease Research:
(5,6-DICHLORO-1,3-DIOXO-1,3-DIHYDRO-ISOINDOL-2-YL)-ACETIC ACID is used in research for its potential role in the treatment of cardiovascular diseases, exploring its effects on various physiological processes related to heart health.
Used in Cancer Therapy Development:
(5,6-DICHLORO-1,3-DIOXO-1,3-DIHYDRO-ISOINDOL-2-YL)-ACETIC ACID is used in the development of cancer therapies, with ongoing studies investigating its potential to target and treat various types of cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 111104-25-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,1,0 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 111104-25:
(8*1)+(7*1)+(6*1)+(5*1)+(4*0)+(3*4)+(2*2)+(1*5)=47
47 % 10 = 7
So 111104-25-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H5Cl2NO4/c11-6-1-4-5(2-7(6)12)10(17)13(9(4)16)3-8(14)15/h1-2H,3H2,(H,14,15)/p-1

111104-25-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(5,6-dichloro-1,3-dioxoisoindol-2-yl)acetic acid

1.2 Other means of identification

Product number -
Other names 4,5-Dichlorophthalimidoacetic acid

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:111104-25-7 SDS

111104-25-7Relevant academic research and scientific papers

DERIVATIVES OF 1-PHENYL-2-PYRIDINYL ALKYL ALCOHOLS AS PHOSPHODIESTERASE INHIBITORS

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Paragraph 0474, (2013/05/08)

Compounds, pyridine N-oxides, and pharmaceutically acceptable salts of formula (I) are useful as inhibitors of the phosphodiesterase 4 (PDE4) enzyme and for preventing and/ or treating diseases of the respiratory tract characterized by airway obstruction, such as asthma or COPD.

DERIVATIVES OF 1-PHENYL-2-PYRIDINYL ALKYL ALCOHOLS AS PHOSPHODIESTERASE INHIBITORS

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Page/Page column 114, (2013/05/09)

The invention relates to inhibitors of the phosphodiesterase 4 (PDE4) enzyme. More particularly, the invention relates to compounds that are derivatives of 1-phenyl-2-pyridinyl alkyl alcohols, methods of preparing such compounds, compositions containing them and therapeutic use thereof.

Cyclic imides; 15. Reaction of 4,5-dichlorophthalimides with potassium nitrite: Synthesis of 4-hydroxy-nitrophthalimides

Caswell,Guevara,Corley,Martinez,Hollis,Largess,Thornley

, p. 823 - 825 (2007/10/02)

N-Substituted 4,5-dichlorophthalimides react with potassium nitrite in refluxing dimethylformamide to form N-substituted 4-hydroxy-5-nitrophthalimides.

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