2437-08-3 Usage
Description
INDAN-2 2-DICARBOXYLIC ACID 97 is a versatile chemical compound with the chemical formula C10H8O4 and a molecular weight of 192.17 g/mol. It is a dicarboxylic acid that is commonly used in the production of pharmaceuticals, polymers, and agrochemicals. INDAN-2 2-DICARBOXYLIC ACID 97 is known for its ability to form stable complexes with metal ions, making it useful in coordination chemistry and as a chelating agent. It is also used in the production of specialty chemicals and as a research reagent in chemical laboratories.
Uses
Used in Pharmaceutical Industry:
INDAN-2 2-DICARBOXYLIC ACID 97 is used as a building block in the synthesis of various organic compounds, such as indan derivatives, which have potential applications in the development of pharmaceuticals.
Used in Polymer Industry:
This chemical compound is used in the production of polymers, which have a wide range of applications in various industries, including plastics, textiles, and coatings.
Used in Agrochemical Industry:
INDAN-2 2-DICARBOXYLIC ACID 97 is used in the production of agrochemicals, which are chemicals used in agriculture to enhance crop productivity and protect crops from pests and diseases.
Used in Coordination Chemistry:
Due to its ability to form stable complexes with metal ions, INDAN-2 2-DICARBOXYLIC ACID 97 is used as a chelating agent in coordination chemistry, which has applications in various fields, including catalysis, materials science, and supramolecular chemistry.
Used in Specialty Chemicals Production:
INDAN-2 2-DICARBOXYLIC ACID 97 is also used in the production of specialty chemicals, which are high-value chemicals used in specific applications, such as fragrances, dyes, and fine chemicals.
Used as a Research Reagent:
INDAN-2 2-DICARBOXYLIC ACID 97 serves as a research reagent in chemical laboratories, where it is used for the synthesis and study of various organic compounds and their properties.
Check Digit Verification of cas no
The CAS Registry Mumber 2437-08-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,3 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2437-08:
(6*2)+(5*4)+(4*3)+(3*7)+(2*0)+(1*8)=73
73 % 10 = 3
So 2437-08-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H10O4/c12-9(13)11(10(14)15)5-7-3-1-2-4-8(7)6-11/h1-4H,5-6H2,(H,12,13)(H,14,15)
2437-08-3Relevant articles and documents
Synthesis of Functionalized Cyclopropindenes via the Carbene Addition Route
Mueller, Paul,Miao, Zhongshan
, p. 2051 - 2059 (1994)
The synthesis of 4,5-dihydro-1H,3H-cycloprop(f)inden-4-ol (1) and diethyl 4,5-dihydro-1H,3H-cyclopropindene-4,4-dicarboxylate 26 starting from diene 4 is described.The cyclopentene ring is constructed by condensation of diethyl malonate to the dibromide 21.The key-step in the synthesis of 1 consists in a twofold Curtius degradation of 22, with subsequent reduction of the carbonyl group and aromatization.The skeleton of the isomer 31 is synthesized via cycloaddition of butadiene to cyclopent-4-ene-1,3-dione (7) and addition of dichlorocarbene to the adduct 27 after ketalization.The attempted synthesis of dihydrocyclopropindene (2) by base-induced elimination of several appropriately substituted precursors failed.
Copper(II)-catalyzed enantioselective intramolecular cyclization of N-alkenylureas
Fu, Shaomin,Yang, Honghao,Deng, Yuanfu,Jiang, Huanfeng,Zeng, Wei,Li, Guoqiang
supporting information, p. 1018 - 1021 (2015/03/30)
The first Cu(II)-catalyzed highly enantioselective intramolecular cyclization of N-alkenylureas was developed for the concise assembly of chiral vicinal diamino bicyclic heterocycles. Facile removal of carbonyl group of the carbamido moiety allowed for ready access to enantioenriched cyclic vicinal diamines.
XANTHINE DERIVATIVES AS ADENOSINE A1 RECEPTOR ANTAGONISTS
-
, (2008/06/13)
A method of attenuating a cognitive deficit in a patient in need thereof comprising administering to the patient a xanthine derivative.
