CAS 18372-22-0
:Methyl indolyl-3-glyoxylate
Description:
Methyl indolyl-3-glyoxylate is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. This compound features a glyoxylate moiety, which contributes to its reactivity and potential applications in organic synthesis. Methyl indolyl-3-glyoxylate is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its structure allows for various chemical transformations, making it of interest in medicinal chemistry and the development of pharmaceuticals. The presence of both the indole and glyoxylate functionalities suggests potential biological activity, which could be explored in drug discovery. As with many organic compounds, safety precautions should be taken when handling methyl indolyl-3-glyoxylate, including the use of appropriate personal protective equipment and adherence to safety data sheet guidelines. Overall, this compound represents a versatile building block in synthetic organic chemistry.
Formula:C11H9NO3
InChI:InChI=1/C11H9NO3/c1-15-11(14)10(13)8-6-12-9-5-3-2-4-7(8)9/h2-6,12H,1H3
SMILES:COC(=O)C(=O)c1c[nH]c2ccccc12
Synonyms:- Methyl 3-Indoleglyoxylate
- Methyl (Indol-3-Yl)Oxoacetate
- Indole-3-Glyoxylic Acid Methyl Ester
- Indole-3-Glyoxylic Methyl Ester
- Methylindole-3-glyoxylate
- IGA-OMe
- methyl 1H-indol-3-yl(oxo)acetate
- Methyl 2-(1H-indol-3-yl)-2-oxoacetate
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Found 7 products.
Methyl 2-(1H-indol-3-yl)-2-oxoacetate
CAS:Formula:C11H9NO3Purity:96%Color and Shape:SolidMolecular weight:203.1941Methyl 3-Indoleglyoxylate
CAS:Formula:C11H9NO3Purity:>96.0%(GC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:203.20Methyl Indolyl-3-glyoxylate
CAS:Controlled ProductFormula:C11H9NO3Color and Shape:NeatMolecular weight:203.19Indole-3-glyoxylic acid methyl ester
CAS:<p>Indole-3-glyoxylic acid methyl ester is a fine chemical that is used as a building block in the synthesis of complex compounds. It can be used in the production of research chemicals, reagents, and specialty chemicals. The CAS number for indole-3-glyoxylic acid methyl ester is 18372-22-0. This compound is a versatile building block that can be used as a reaction component or scaffold for the synthesis of other compounds.</p>Formula:C11H9NO3Purity:98.0 To 100.0 Area-%Molecular weight:203.20 g/molRef: 3D-I-2810
25gTo inquire50gTo inquire100gTo inquire250gTo inquire500gTo inquire-Unit-ggTo inquireMethyl indolyl-3-glyoxylate
CAS:<p>Methyl indolyl-3-glyoxylate is an active analogue of hepg2, a protein involved in the synthesis of prenylated proteins. It inhibits the prenylation of proteins and halides by binding to ATP, preventing the formation of a covalent bond between ATP and the protein. Methyl indolyl-3-glyoxylate has been shown to induce apoptosis in HeLa cells by inhibiting cell proliferation and DNA synthesis. This compound also causes g1 phase arrest, which may be due to its ability to alkylate DNA. Methyl indolyl-3-glyoxylate has also been shown to be effective against cancer cells in vitro and in vivo, particularly those that are resistant to other chemotherapeutic drugs.</p>Formula:C11H9NO3Purity:Min. 95%Color and Shape:PowderMolecular weight:203.19 g/molMethyl 2-(1H-indol-3-yl)-2-oxoacetate
CAS:Formula:C11H9NO3Purity:96%Color and Shape:SolidMolecular weight:203.197





