CAS 42399-49-5
:(2S,3S)-3-Idrossi-2-(4-metossifenil)-2,3-diidro-1,5-benzotiazepin-4(5H)-one
Descrizione:
(2S,3S)-3-Idrossi-2-(4-metossifenil)-2,3-diidro-1,5-benzotiazepin-4(5H)-one è un composto chimico caratterizzato dalla sua complessa struttura biciclica, che include un nucleo di benzotiazepina. Questo composto presenta un gruppo idrossile nella posizione 3 e un gruppo fenilico sostituito da metossile nella posizione 2, contribuendo alla sua potenziale attività biologica. La stereochimica indicata da (2S,3S) suggerisce disposizioni spaziali specifiche dei suoi atomi, che possono influenzare significativamente le sue interazioni e reattività. La presenza della porzione di benzotiazepina spesso si correla con varie proprietà farmacologiche, inclusi effetti potenziali sul sistema nervoso centrale. Il numero CAS del composto, 42399-49-5, consente un'identificazione precisa nei database chimici. La sua solubilità, stabilità e reattività dipenderebbero dalle condizioni specifiche, come pH e solvente, rendendolo importante per applicazioni in chimica medicinale e sviluppo di farmaci. In generale, questo composto rappresenta uno scaffold unico che può essere esplorato per usi terapeutici.
Formula:C16H15NO3S
InChI:InChI=1S/C16H15NO3S/c1-20-11-8-6-10(7-9-11)15-14(18)16(19)17-12-4-2-3-5-13(12)21-15/h2-9,14-15,18H,1H3,(H,17,19)/t14-,15+/m1/s1
InChI key:InChIKey=LHBHZALHFIQJGJ-CABCVRRESA-N
SMILES:O[C@@H]1[C@@H](SC=2C(NC1=O)=CC=CC2)C3=CC=C(OC)C=C3
Sinonimi:- (2S,3S)-2,3-Dihydro-3-hydroxy-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one
- (2S,3S)-3-Hydroxy-2-(4-Methoxy-Phenyl)-2,3-Dihydro-5H-Benzo[B][1,4]Thiazepin-4-One
- (2S,3S)-3-hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-1,5-benzothiazepin-4(5H)-one
- (2S-Cis)-(+)-Dihydro-3-Oh-2-(4-Meo-Ph)-1 ,5-Benzothiazepin-4(5H)-One, 98%
- 1,5-Benzothiazepin-4(5H)-one, 2,3-dihydro-3-hydroxy-2-(4-methoxyphenyl)-, (2S,3S)-
- 1,5-Benzothiazepin-4(5H)-one, 2,3-dihydro-3-hydroxy-2-(4-methoxyphenyl)-, (2S-cis)-
- 5-Benzothiazepin-4(5H)-One,2,3-Dihydro-3-Hydroxy-2-(4-Methoxyphenyl)-(2S-C
- Cis (+) Hydroxy Lactam
- Cis-2,3-Dihydro-3-Hydroxy-2-(4-Methoxyphenyl)-1,5-Benzothiazepin-4(5H)-One
- Hydroxy Lactam
Ordinare per
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10 prodotti.
(2S,3S)-2,3-Dihydro-3-hydroxy-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one
CAS:Formula:C16H15NO3SPurezza:97%Colore e forma:SolidPeso molecolare:301.3602(2S-Cis)-(+)-2,3-Dihydro-3-Hydroxy-2-(4-Methoxyphenyl)-1,5-Benzothiazepin-4(5H)-One
CAS:(2S-Cis)-(+)-2,3-Dihydro-3-Hydroxy-2-(4-Methoxyphenyl)-1,5-Benzothiazepin-4(5H)-OnePurezza:99%Peso molecolare:301.36g/mol(2S,3S)-(+)-2,3-Dihydro-3-hydroxy-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one
CAS:Formula:C16H15NO3SPurezza:>96.0%(HPLC)(N)Colore e forma:White to Light yellow powder to crystalPeso molecolare:301.36(2S,3S)-3-Hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-1,5-benzothiazepin-4(5H)-one
CAS:Prodotto controllatoFormula:C16H15NO3SColore e forma:NeatPeso molecolare:301.36Des[3-Acetyl-5-(2-dimethylamino)ethyl] Diltiazem
CAS:Prodotto controllato<p>Applications A key intermediate for Diltiazem (D460620) synthesis.<br>References Nagao, T., et al.: Jpn. J. Pharmacol., 22, 1 (1972), Senuma, M., et al.: Chem. Pharm. Bull., 37, 3204 (1989), Kometani, T., et al.: J. Ferment. Bioeng., 80, 208 (1995),<br></p>Formula:C16H15NO3SColore e forma:NeatPeso molecolare:301.36(2S,3S)-3-Hydroxy-2-(4-methoxyphenyl)-2,3-dihydrobenzo[b][1,4]thiazepin-4(5H)-one
CAS:Purezza:95.0%Peso molecolare:301.3599853515625Ref: ST-EA-CP-D22005
10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaDes[3-acetyl-5-(2-dimethylamino)ethyl] diltiazem
CAS:<p>Diltiazem is an anti-anginal agent that belongs to the group of calcium channel blockers. It is used to treat chest pain (angina) due to coronary artery disease and other conditions. Diltiazem is a racemic mixture of two enantiomers, (+)-diltiazem and (-)-diltiazem. The synthesis of diltiazem from (+)-diltiazem has been reported by asymmetric synthesis with a chiral catalyst. In this process, irradiation of the reaction mixture at 254 nm converts the nitro group in the molecule into an anisaldehyde group, which can be cleaved by nucleophilic substitution with phenylmethyl sulfide. This high yield, efficient method produces diltiazem hydrochloride as a white solid that crystallizes in needles or crystals.</p>Formula:C16H15NO3SPurezza:Min. 95%Colore e forma:Beige PowderPeso molecolare:301.36 g/mol(2S,3S)-3-Hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-1,5-benzothiazepin-4(5H)-one
CAS:Colore e forma:Neat
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