100986-86-5 | (R)-Ofloxacin

Packsize	Purity	Availability	Price	Discounted Price
5mg	95%	in stock	$48.00	$33.00
10mg	95%	in stock	$65.00	$45.00
25mg	95%	in stock	$128.00	$89.00
50mg	95%	in stock	$215.00	$150.00
100mg	95%	in stock	$312.00	$218.00
250mg	95%	in stock	$463.00	$324.00

Description

• Catalog Number: AA04181
• Chemical Name: (R)-Ofloxacin
• CAS Number: 100986-86-5
• Molecular Formula: C18H20FN3O4
• Molecular Weight: 361.3675
• MDL Number: MFCD00869643
• SMILES: CN1CCN(CC1)c1c(F)cc2c3c1OC[C@H](n3cc(c2=O)C(=O)O)C

Upstream Synthesis Route

(3R)-9-Fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid is a versatile compound that finds wide application in chemical synthesis processes. Its unique structure and functional groups make it a valuable building block for the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals.In chemical synthesis, this compound can serve as a key intermediate in the preparation of complex drug molecules due to its ability to undergo multiple functional group transformations. Its fluorine substituent can participate in various reactions such as nucleophilic substitution or transition metal-catalyzed cross-coupling reactions, enabling the introduction of fluorine-containing motifs into the final product. The presence of the piperazine moiety provides opportunities for further modifications or derivatizations through selective functionalization, allowing for the creation of diverse chemical libraries.Moreover, the carboxylic acid group in (3R)-9-Fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid can act as a handle for conjugation with other molecules or solid supports in peptide coupling reactions or drug conjugation strategies. This feature enhances the compound's utility in the construction of bioconjugates and prodrugs, expanding its applications in medicinal chemistry and drug delivery systems.Overall, (3R)-9-Fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid demonstrates considerable potential as a versatile tool in the arsenal of synthetic chemists for the efficient and strategic assembly of diverse molecular architectures with relevance in various scientific disciplines.