CAS 5728-15-4
:3-(cyclopentylmethyl)-2-(ethylsulfanyl)-3H-spiro[benzo[h]quinazoline-5,1'-cyclopentan]-4(6H)-one
Description:
3-(Cyclopentylmethyl)-2-(ethylsulfanyl)-3H-spiro[benzo[h]quinazoline-5,1'-cyclopentan]-4(6H)-one, with the CAS number 5728-15-4, is a complex organic compound characterized by its spirocyclic structure, which incorporates both a quinazoline and a cyclopentanone moiety. This compound features a cyclopentylmethyl group and an ethylsulfanyl substituent, contributing to its unique chemical properties. The presence of sulfur in the ethylsulfanyl group can influence the compound's reactivity and solubility, while the spiro arrangement may impart specific steric and electronic characteristics. Such compounds often exhibit interesting biological activities, making them of interest in medicinal chemistry. The molecular structure suggests potential for interactions with biological targets, which could be explored in drug development. Additionally, the compound's stability and reactivity can be influenced by factors such as pH, temperature, and solvent, which are important considerations in both synthetic and application contexts. Overall, this compound exemplifies the complexity and diversity found in organic chemistry, particularly in the realm of heterocyclic compounds.
Formula:C24H30N2OS
InChI:InChI=1/C24H30N2OS/c1-2-28-23-25-21-19-12-6-5-11-18(19)15-24(13-7-8-14-24)20(21)22(27)26(23)16-17-9-3-4-10-17/h5-6,11-12,17H,2-4,7-10,13-16H2,1H3
SMILES:CCSc1nc2c3ccccc3CC3(CCCC3)c2c(=O)n1CC1CCCC1
Synonyms:- Spiro[benzo[h]quinazoline-5(3H),1'-cyclopentan]-4(6H)-one, 3-(cyclopentylmethyl)-2-(ethylthio)-
- 3-(Cyclopentylmethyl)-2-(ethylsulfanyl)-3H-spiro[benzo[h]quinazoline-5,1'-cyclopentan]-4(6H)-one
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Found 3 products.
4-Chloro-3-hydroxy-1,2,5-thiadiazole
CAS:4-Chloro-3-hydroxy-1,2,5-thiadiazolePurity:97%Color and Shape:SolidMolecular weight:136.56g/mol4-Chloro-1,2,5-thiadiazol-3-ol
CAS:<p>4-Chloro-1,2,5-thiadiazol-3-ol is an antibacterial agent that belongs to the class of imidazolidinones. It inhibits the growth of bacteria by reacting with sulfur in their cell walls and chlorinating them. 4-Chloro-1,2,5-thiadiazol-3-ol has been shown to be effective against a wide range of bacteria including Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, and Enterobacter cloacae. 4-Chloro-1,2,5-thiadiazol 3-ol also has been shown to react with chloride ions in body fluids and form hydrochloric acid which may be responsible for some of its antibacterial activity.</p>Formula:C2HClN2OSPurity:Min. 95%Color and Shape:PowderMolecular weight:136.56 g/mol



