Ethyl 5-Hydroxy-2-methylindole-3-carboxylate

CAS: 7598-91-6

Ref. 3D-FE56798

Produktinformation

• Name: Ethyl 5-Hydroxy-2-methylindole-3-carboxylate
• Synonyme: 3-Carbethoxy-5-hydroxy-2-methylindole5-Hydroxy-2-methyl-1H-indole-3-carboxylic acid ethyl ester, 1H-Indole-3-carboxylic acid, 5-hydroxy-2-methyl-, ethyl ester, 2-Methyl-3-carbethoxy-5-hydroxyindole, 3-(Ethoxycarbonyl)-2-methyl-5-hydroxyindole, 3-Ethoxycarbonyl-5-hydroxy-2-methylindole, 5-Hydroxy-2-methyl-1H-indole-3-carboxylic acid ethyl ester, 5-Hydroxy-2-methyl-3-indolecarboxylic acid ethyl ester, Indole-3-carboxylic acid, 5-hydroxy-2-methyl-, ethyl ester, NSC 405600, ethyl 5-hydroxy-2-methyl-1H-indole-3-carboxylate

Beschreibung

Ethyl 5-hydroxy-2-methylindole-3-carboxylate is a drug target, which is an active methylene that can be detected in the human brain. It may also play a role in cognition and functional groups. Ethyl 5-hydroxy-2-methylindole-3-carboxylate is a quinone, which is an organic compound with two hydroxy groups and one carbonyl group. Quinones are used agriculturally and synthetic methods are used to produce this product. The synthesis of ethyl 5-hydroxy-2-methylindole 3 carboxylate involves the use of serotonin as a starting material, which is then reacted with acetic acid to form acetoacetic ester. This reaction also requires potassium hydroxide as a base and chloroacetone as an acid catalyst. This product has been shown to have antiperoxidative properties and can be used for the treatment of fun

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 219.24 g/mol
• Formel: C₁₂H₁₃NO₃
• Reinheit: Min. 95%
• InChl: InChI=1S/C12H13NO3/c1-3-16-12(15)11-7(2)13-10-5-4-8(14)6-9(10)11/h4-6,13-14H,3H2,1-2H3
• InChI Key: InChIKey=BSNHKSUAAMJXBB-UHFFFAOYSA-N
• SMILES: CCOC(=O)c1c(C)[nH]c2ccc(O)cc12