110317-55-0 Usage
Description
(E)-2-(3-Indolyl)-2-(hydroxyimino)essigsaeure-methylester is a chemical compound that is commonly used in research and chemical synthesis. It is classified as a methyl ester and is derived from (E)-2-(3-Indolyl)-2-(hydroxyimino)essigsaeure, which is a compound with potential antineoplastic and antitumor properties. This chemical has also been studied for its potential use in the treatment of diseases such as cancer and neurological disorders. The exact mechanism of action of (E)-2-(3-Indolyl)-2-(hydroxyimino)essigsaeure-methylester is still being investigated, but it is believed to have an impact on various biochemical processes within the body. Due to its potential medicinal properties, this compound is a subject of ongoing research and development in the field of pharmaceuticals and biotechnology.
Uses
Used in Pharmaceutical Research:
(E)-2-(3-Indolyl)-2-(hydroxyimino)essigsaeure-methylester is used as a research compound for its potential antineoplastic and antitumor properties. (E)-2-(3-Indolyl)-2-(hydroxyimino)essigsaeure-methylester is being investigated for its ability to impact various biochemical processes within the body, which may contribute to the development of new treatments for cancer and neurological disorders.
Used in Chemical Synthesis:
(E)-2-(3-Indolyl)-2-(hydroxyimino)essigsaeure-methylester is used as a synthetic building block in the creation of other chemical compounds. Its unique structure and reactivity make it a valuable component in the synthesis of various molecules, particularly those with potential applications in the pharmaceutical and biotechnology industries.
Used in Drug Development:
(E)-2-(3-Indolyl)-2-(hydroxyimino)essigsaeure-methylester is used as a starting material in the development of new drugs. Its potential medicinal properties make it a promising candidate for further research and development, with the aim of creating novel therapeutic agents for the treatment of various diseases, including cancer and neurological disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 110317-55-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,3,1 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 110317-55:
(8*1)+(7*1)+(6*0)+(5*3)+(4*1)+(3*7)+(2*5)+(1*5)=70
70 % 10 = 0
So 110317-55-0 is a valid CAS Registry Number.
110317-55-0Relevant articles and documents
Alboinon, an oxadiazinone alkaloid from the ascidian Dendrodoa grossularia
Bergmann, Tanja,Schories, Dirk,Steffan, Bert
, p. 2055 - 2060 (1997)
The ascidian Dendrodoa grossularia, collected in the Baltic Sea, contains the new 1,3,5-oxadiazin-2-one alkaloid alboinon (1).
Hexahydropyrroloindoles - Attempts to Synthesize 2-Indolyl Thioethers
Droste, Holger,Wieland, Theodor
, p. 901 - 910 (2007/10/02)
The N-tryptamine derivatives 9, 11, 12, and 19 with the functional groups CN, CONH2, CO2H, and CO2Me, respectively, in the α position to the indole ring have been synthesized.Sensitized photooxiation of 9, 12, 19, N-Boc--tryptophan (21), and N-Boc-tryptamine (22) affords the hexahydropyrroloindoles 23-27, in the case of 11 the ring closure occurs at the amine nitrogen to give the ketone 28, N-Boc-homotryptamine (31) yields the hexahydropyridoindole 32, whereas no azetidine formation from 2-(3-indolyl)glycine (36) is observed.The oxi mes 34a and 34 b, intermediates in the synthesis of 36, have been separated chromatographically and characterized NMR spectroscopically as E and Z-isomers, respectively.- Attempts to introduce with cysteine derivatives a thioether group in position 2 of the compounds described above, failed. 21, 22, 26, 27, and N-Boc-2-(3-indolyl)propylamine (43), bearing a methyl group in the α position to the indole ring, and its photooxidation product 44 show only thin-layer chromatographically detectable thioether formation.
