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Merck

194123

Benzimidazole

98%

Synonym(s):

1,3-Benzodiazole, BZI

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About This Item

Empirical Formula (Hill Notation):
C7H6N2
CAS Number:
51-17-2
Molecular Weight:
118.14
NACRES:
NA.22
PubChem Substance ID:
24851632
eCl@ss:
32151902
UNSPSC Code:
12352100
EC Number:
200-081-4
MDL number:
MFCD00005585
Beilstein/REAXYS Number:
109682
Assay:
98%
Form:
powder

Key Documents

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InChI key

HYZJCKYKOHLVJF-UHFFFAOYSA-N

InChI

1S/C7H6N2/c1-2-4-7-6(3-1)8-5-9-7/h1-5H,(H,8,9)

SMILES string

c1ccc2[nH]cnc2c1

assay

98%

form

powder

Quality Level

200

mp

169-171 °C (lit.)

solubility

xylene: soluble 1g in 2g (boiling)(lit.), alcohol: freely soluble(lit.), benzene: insoluble(lit.), cold water: very slightly soluble(lit.), diethyl ether: very slightly soluble(lit.), petroleum ether: insoluble(lit.), water: soluble (hot)(lit.)

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Application

Benzimidazole was used as template compound in the preparation of molecularly imprinted polymer via electropolymerization and electrodeposition of pyrrole on a pencil graphite electrode. It was also used in the preparation of benzimidazolium surfactant, 1-hexadecyl-1H-benzimidazole.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB2977
STBL2607
STBL0182
STBK7957
STBK5963

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Nevine M Y Elsayed et al.
Bioorganic chemistry, 82, 340-359 (2018-11-15)
VEGFR-2 has a pivotal role in promoting cancer angiogenesis. Herein, two series of novel indazole-based derivatives were designed, synthesized and evaluated for their in vitro inhibitory action against VEGFR-2 kinase enzyme. The second series 11a-e exhibited better potency than the
Benzimidazolium surfactants for modification of clays for use with styrenic polymers.
Costache MC, et al.
Polymer Degradation and Stability, 92(10), 1753-1762 (2007)
Stephan Mokesch et al.
Molecules (Basel, Switzerland), 24(13) (2019-06-30)
Fine-tuning of the properties of a recently reported 1,3-indandione-based organoruthenium complex is attempted to optimize the stability under physiological conditions. Previous work has shown its capacity of inhibiting topoisomerase IIα; however, fast aquation leads to undesired reactions and ligand cleavage
Magdalena J Mazur et al.
Plant physiology, 179(1), 168-183 (2018-11-06)
Attachment of the small ubiquitin-like modifier (SUMO) to substrate proteins modulates their turnover, activity, or interaction partners. However, how this SUMO conjugation activity concentrates the proteins involved and the substrates into uncharacterized nuclear bodies (NBs) remains poorly understood. Here, we
Moshe Ronen et al.
Pathogens (Basel, Switzerland), 8(4) (2019-12-05)
Net blotch (NB) is a major disease of barley caused by the fungus Pyrenophora teres f. teres (Ptt), and P. teres f. maculata (Ptm). Ptt and Ptm infect the cultivated crop (Hordeum vulgare) and its wild relatives (H. vulgare ssp.
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