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BCR136R

Benzo[b]naphtho[2,3-d]thiophene

BCR®, certified reference material

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About This Item

Empirical Formula (Hill Notation):
C16H10S
CAS Number:
243-46-9
Molecular Weight:
234.32
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329774225
MDL number:
MFCD00143667
Beilstein/REAXYS Number:
157102

Key Documents

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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

SMILES string

c1ccc2cc3c(cc2c1)sc4ccccc34

InChI key

UWMISBRPSJFHIR-UHFFFAOYSA-N

grade

certified reference material

agency

BCR®

manufacturer/tradename

JRC

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

format

neat

storage temp.

2-8°C

Related Categories

Analysis Note

For more information please see:
BCR136R

Legal Information

BCR is a registered trademark of European Commission

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

hcodes

H302,H410

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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