111104-25-7 Usage
General Description
(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 used in the pharmaceutical industry. It belongs to the class of organic compounds known as phenoxyacetic acid derivatives and is commonly used in 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 useful in the treatment of autoimmune diseases and conditions characterized by abnormal immune responses. It is also being studied for its potential use in the treatment of cardiovascular diseases and cancer. Overall, (5,6-DICHLORO-1,3-DIOXO-1,3-DIHYDRO-ISOINDOL-2-YL)-ACETIC ACID plays a crucial role in drug development and medical research.
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
111104-25-7Relevant articles and documents
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.
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.
