163769-88-8 Usage
Uses
Used in Pharmaceutical Industry:
5,6-DIHYDRO-2,3-DIMETHOXY-6,6-DIMETHYLBENZ[7,8]INDOLIZINO[2,3-B]QUINOXALINE is used as a pharmaceutical agent for the development of new drugs. Its unique molecular structure and chemical properties make it a promising candidate for the treatment of various diseases and disorders.
Used in Chemical Research:
5,6-DIHYDRO-2,3-DIMETHOXY-6,6-DIMETHYLBENZ[7,8]INDOLIZINO[2,3-B]QUINOXALINE is used as a research compound in the field of organic chemistry. It can be employed to study the synthesis, properties, and reactions of complex organic molecules, contributing to the advancement of chemical knowledge and the development of new chemical processes.
Used in Material Science:
5,6-DIHYDRO-2,3-DIMETHOXY-6,6-DIMETHYLBENZ[7,8]INDOLIZINO[2,3-B]QUINOXALINE can be used in the development of new materials with unique properties. Its chemical structure and functional groups can be utilized to create novel materials with potential applications in various industries, such as electronics, energy, and environmental protection.
Used in Analytical Chemistry:
5,6-DIHYDRO-2,3-DIMETHOXY-6,6-DIMETHYLBENZ[7,8]INDOLIZINO[2,3-B]QUINOXALINE can be employed as an analytical reagent or standard in various analytical techniques, such as chromatography, spectroscopy, and electrochemistry. Its unique chemical properties can be utilized to improve the sensitivity, selectivity, and accuracy of these analytical methods.
Used in Environmental Applications:
5,6-DIHYDRO-2,3-DIMETHOXY-6,6-DIMETHYLBENZ[7,8]INDOLIZINO[2,3-B]QUINOXALINE can be used in environmental applications, such as the detection and removal of pollutants, the degradation of hazardous substances, and the development of eco-friendly materials. Its unique chemical properties can contribute to the development of innovative solutions for environmental challenges.
Biological Activity
Novel, selective inhibitor of interleukin-5 (IL-5) binding to its receptor (IC 50 = 0.45-1 mM). Inhibits IL-5-prolonged eosinophil survival and IL-5-induced tyrosine phosphorylation of JAK2 without inhibiting GM-CSF-mediated effects. In vivo, inhibits antigen-induced eosinophil and lymphocyte recruitment in rat airways, without affecting peripheral blood or bone marrow leukocytes.
Check Digit Verification of cas no
The CAS Registry Mumber 163769-88-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,7,6 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 163769-88:
(8*1)+(7*6)+(6*3)+(5*7)+(4*6)+(3*9)+(2*8)+(1*8)=178
178 % 10 = 8
So 163769-88-8 is a valid CAS Registry Number.
InChI:InChI=1/C22H21N3O2/c1-22(2)12-13-9-19(26-3)20(27-4)10-14(13)18-11-17-21(25(18)22)24-16-8-6-5-7-15(16)23-17/h5-11H,12H2,1-4H3
163769-88-8Relevant articles and documents
REACTION OF ENAMINES OF THE ISOCHOLINE AND PHENANTHRIDINE SERIES WITH OXALYL CHLORIDE
Mikhailovskii, A.G.,Shklyeav, V.S.
, p. 818 - 821 (2007/10/02)
Compounds of the 2,3-dioxopyrroloisoquinoline and 2,3-dioxopyrrolophenanthridine series were synthesized and the products of their codensation with o-phenylenediamine were obtained.
