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BCR137R

苯并[b]萘并[1,2-d]噻吩

BCR®, certified reference material

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About This Item

经验公式（希尔记法）:
C16H10S
CAS号:
205-43-6
分子量:
234.32
Beilstein:
9635
MDL编号:
MFCD00215942
UNSPSC代码:
41116107
PubChem化学物质编号:
329774226
NACRES:
NA.24

等级

certified reference material

Agency

BCR®

制造商/商品名称

JRC

技术

HPLC: suitable
gas chromatography (GC): suitable

格式

neat

储存温度

2-8°C

SMILES字符串

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

InChI key

XZUMOEVHCZXMTR-UHFFFAOYSA-N

相关类别

分析说明

For more information please see:
BCR137R

法律信息

BCR is a registered trademark of European Commission

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

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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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