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Merck
CN

BCR136R

苯并[b]萘并[2,3-d]噻吩

BCR®, certified reference material

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关于此项目

经验公式(希尔记法):
C16H10S
化学文摘社编号:
分子量:
234.32
Beilstein:
157102
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24
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等级

certified reference material

Agency

BCR®

制造商/商品名称

JRC

技术

HPLC: suitable
gas chromatography (GC): suitable

包装形式

neat

储存温度

2-8°C

SMILES字符串

c1ccc2cc3c(cc2c1)sc4ccccc34

InChI

1S/C16H10S/c1-2-6-12-10-16-14(9-11(12)5-1)13-7-3-4-8-15(13)17-16/h1-10H

InChI key

UWMISBRPSJFHIR-UHFFFAOYSA-N

分析说明

For more information please see:
BCR136R

法律信息

BCR is a registered trademark of European Commission

象形图

Exclamation markEnvironment

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Hannie S van der Honing et al.
The New phytologist, 185(1), 90-102 (2009-09-19)
Here, we produced cytoplasmic protrusions with optical tweezers in mature BY-2 suspension cultured cells to study the parameters involved in the movement of actin filaments during changes in cytoplasmic organization and to determine whether stiffness is an actin-related property 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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