BCR137R
Benzo[b]naphtho[1,2-d]thiophene
BCR®, certified reference material
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About This Item
Formula empirica (notazione di Hill):
C16H10S
Numero CAS:
Peso molecolare:
234.32
Beilstein:
9635
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24
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Grado
certified reference material
agenzia
BCR®
Produttore/marchio commerciale
JRC
tecniche
HPLC: suitable
gas chromatography (GC): suitable
Formato
neat
Temperatura di conservazione
2-8°C
Stringa SMILE
c1ccc2c(c1)ccc3sc4ccccc4c23
InChI
1S/C16H10S/c1-2-6-12-11(5-1)9-10-15-16(12)13-7-3-4-8-14(13)17-15/h1-10H
XZUMOEVHCZXMTR-UHFFFAOYSA-N
Risultati analitici
For more information please see:
BCR137R
BCR137R
Note legali
BCR is a registered trademark of European Commission
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
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Certificati d'analisi (COA)
Lot/Batch Number
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Jose Juan Rodríguez et al.
Organic & biomolecular chemistry, 10(36), 7334-7346 (2012-08-01)
Based on the benzo[b]naphtho[1,2-d]furan and benzo[b]naphtho[1,2-d]thiophene frameworks, a series of ligands with different basic side chains (BSCs) has been synthesized and pharmacologically evaluated. Also, their binding modes have been modelled using docking techniques. It was found that the introduction of
J Jacob et al.
Cancer letters, 32(1), 107-116 (1986-07-01)
Thiaarenes are metabolized by liver microsomes of untreated rats predominantly to sulfones and sulfoxides. After pretreatment of rats with monooxygenase inducers, ring oxidation of thiaarenes is also observed. In case of benzo[b]naphtho[2,3-d]thiophene the formation of a p-quinone takes place. Rat
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