1193314-23-6 | Spiro[3h-indole-3,1'-[1h]pyrido[3,4-b]indol]-2(1h)-one, 5,7'-dichloro-6'-fluoro-2',3',4',9'-tetrahydro-3'-methyl-, (1'r,3's)-

Packsize	Purity	Availability	Price	Discounted Price
1mg	98%	in stock	$106.00	$74.00
5mg	98%	in stock	$466.00	$326.00
10mg	98%	in stock	$826.00	$578.00

Description

• Catalog Number: AA23930
• Chemical Name: Spiro[3h-indole-3,1'-[1h]pyrido[3,4-b]indol]-2(1h)-one, 5,7'-dichloro-6'-fluoro-2',3',4',9'-tetrahydro-3'-methyl-, (1'r,3's)-
• CAS Number: 1193314-23-6
• Molecular Formula: C19H14Cl2FN3O
• Molecular Weight: 390.2384
• MDL Number: MFCD25976667
• SMILES: C[C@H]1Cc2c3cc(F)c(cc3[nH]c2[C@@]2(N1)C(=O)Nc1c2cc(Cl)cc1)Cl

Upstream Synthesis Route

(1'R,3'S)-5,7'-Dichloro-6'-fluoro-2',3',4',9'-tetrahydro-3'-methylspiro[3H-indole-3,1'-[1H]pyrido[3,4-b]indol]-2(1H)-one, commonly known as $name$, is a highly versatile compound widely utilized in chemical synthesis. This compound serves as a key building block in the creation of complex organic molecules due to its unique structural features and reactivity.$name$ is particularly valuable in the development of pharmaceuticals, agrochemicals, and materials science. Its spirocyclic structure imparts significant rigidity and stereochemical control, making it a valuable tool in the synthesis of chiral compounds. The presence of chloro and fluoro substituents provides opportunities for diverse functional group manipulations, enabling the introduction of various substituents at specific positions in the molecule.In chemical synthesis, $name$ can act as a precursor for the construction of biologically active compounds, such as anticancer agents, antibiotics, or enzyme inhibitors. Its spirocyclic moiety can serve as a scaffold for the design of novel molecules with improved pharmacological properties. Furthermore, the fluorine atom in $name$ enhances the compound's lipophilicity and metabolic stability, making it an attractive candidate for further derivatization and optimization in drug discovery programs.Overall, the strategic incorporation of (1'R,3'S)-5,7'-Dichloro-6'-fluoro-2',3',4',9'-tetrahydro-3'-methylspiro[3H-indole-3,1'-[1H]pyrido[3,4-b]indol]-2(1H)-one in chemical synthesis enables chemists to access a diverse array of molecular architectures with promising biological activities and physicochemical properties.