90347-97-0 Usage
Uses
Used in Pharmaceutical Industry:
Indolizine-1-carboxylic acid is used as a key building block for the synthesis of various pharmaceuticals, leveraging its reactive nature and versatile reactivity to create compounds with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, Indolizine-1-carboxylic acid serves as a crucial component in the development of new agrochemicals, contributing to the creation of effective solutions for pest and disease control in agriculture.
Used in Natural Product Synthesis:
Indolizine-1-carboxylic acid is utilized as a synthetic intermediate for the production of natural products, facilitating the development of novel compounds with potential biological activities.
Used in Organic Light-Emitting Diodes (OLEDs):
Indolizine-1-carboxylic acid is employed as a photoactive material in the development of organic light-emitting diodes, contributing to the advancement of display and lighting technologies.
Used in Organic Solar Cells:
As a photoactive material, Indolizine-1-carboxylic acid is also used in the research and development of organic solar cells, playing a role in the pursuit of more efficient and sustainable energy solutions.
Check Digit Verification of cas no
The CAS Registry Mumber 90347-97-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,4 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90347-97:
(7*9)+(6*0)+(5*3)+(4*4)+(3*7)+(2*9)+(1*7)=140
140 % 10 = 0
So 90347-97-0 is a valid CAS Registry Number.
90347-97-0Relevant academic research and scientific papers
Synthesis of biindolizines through highly regioselective palladium-catalyzed C-H functionalization
Xia, Ji-Bao,Wang, Xue-Qiang,You, Shu-Li
supporting information; experimental part, p. 456 - 458 (2009/04/07)
(Chemical Equation Presented) Biindolizines were synthesized under mild conditions with excellent regioselectivity in high yields through palladium-catalyzed C-H functionalization of indolizines. Synthesis of a macrocyclic compound was also achieved via intramolecular double C-H functionalization.
Synthesis of 3-Haloindolizines by copper(ii) halide mediated direct functionalization of indolizines
Xia, Ji-Bao,You, Shu-Li
supporting information; experimental part, p. 1187 - 1190 (2009/08/07)
3-Haloindolizines were synthesized via Cu(II) halide mediated halogenation of indolizines. This C-H direct functionalization process occurred under mild conditions giving 3-haloindolizines in moderate to excellent yields, and the products obtained were tested under the Suzuki-Miyaura reaction providing 3-arylindolizines in high yields.
INDOLIZINE CARBOXAMIDES AND THE AZA AND DIAZA DERIVATIVES THEREOF
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Page/Page column 50, (2010/10/19)
The invention relates to neuroreceptor-active carboxamide-substituted indolizine derivatives of general formula (I) wherein X represents a group of general formula (X1).
