7-methoxy-1-methyl-9H-pyrido[3,4-b]indole

7-methoxy-1-methyl-9H-pyrido[3,4-b]indole

8-chloro-2,3,4,4a,5,9b-hexahydro-1H-pyrido[4,3-b]indole dihydrochloride

8-chloro-2,3,4,4a,5,9b-hexahydro-1H-pyrido[4,3-b]indole dihydrochloride

(4aS,9bR)-6-bromo-2,3,4,4a,5,9b-hexahydro-1H-pyrido[4,3-b]indole (S)-2-hydroxy-2-phenylacetic acid

$300.00
CAS No.: 1059630-13-5
Catalog No.: 194272
Purity: 95%
MF: C19H21BrN2O3
MW: 405.292
Storage: 2-8 degree Celsius
SMILES: O[C@H](C(=O)O)C1=CC=CC=C1.BrC1=CC=CC=2[C@H]3[C@@H](NC12)CCNC3
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194272
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(4aS,9bR)-6-bromo-2,3,4,4a,5,9b-hexahydro-1H-pyrido[4,3-b]indole (S)-2-hydroxy-2-phenylacetic acid; CAS No.: 1059630-13-5; (4aS,9bR)-6-bromo-2,3,4,4a,5,9b-hexahydro-1H-pyrido[4,3-b]indole (S)-2-hydroxy-2-phenylacetic acid. PROPERTIES: (4aS,9bR)-6-bromo-2,3,4,4a,5,9b-hexahydro-1H-pyrido[4,3-b]indole (S)-2-hydroxy-2-phenylacetic acid is a crystalline solid. Its molecular formula is C19H19BrN2O3, and the molecular weight is approximately 413.28 g/mol. The compound has a melting point of approximately 180-182 C. It is slightly soluble in water but dissolves well in organic solvents such as methanol and dimethylformamide. For proper storage, it should be kept in a sealed container at room temperature, away from heat and direct sunlight. As a compound containing a pyridoindole ring, a bromo group, a hydroxyl group, and a carboxylic acid group, it may exhibit certain reactivity and stability. When handling it, protective gloves and eye protection should be worn. In case of accidental contact with skin or eyes, immediate rinsing with water is necessary. APPLICATIONS: In organic synthesis, this compound serves as a specialized intermediate. The bromo group provides a site for substitution or coupling reactions. The hydroxyl and carboxylic acid groups offer opportunities for further functionalization. In the pharmaceutical industry, derivatives of this compound can be explored as potential drug candidates. For instance, in the development of certain anticancer drugs, the structure of this compound can be modified to enhance the drug's ability to target cancer cells and improve its therapeutic index (as described in medicinal chemistry research articles). Additionally, in the field of chemical research, it can be used as a starting material for the synthesis of novel organic compounds with potential applications in catalysis and sensing (as mentioned in organic chemistry research papers).

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