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Merck
CN

194123

Benzimidazole

98%

Synonym(s):

1,3-Benzodiazole, BZI

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About This Item

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

assay

98%

form

powder

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.)

SMILES string

c1ccc2[nH]cnc2c1

InChI

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

InChI key

HYZJCKYKOHLVJF-UHFFFAOYSA-N

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.


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pictograms

Exclamation mark

signalword

Warning

hcodes

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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Wang Zhang et al.
ACS nano, 14(2), 1971-1981 (2020-01-31)
The development of highly efficient electrocatalysts to reduce overpotentials is vital for accelerating the sluggish oxygen evolution reaction (OER) processes. Herein, we demonstrate ultrathin heterogeneous nanosheets as a promising OER electrocatalyst, which are composed of ultrafine CoFeOx nanoparticles and a
Mohammad Mahdi Najafpour et al.
Dalton transactions (Cambridge, England : 2003), 42(4), 879-884 (2012-11-28)
In this communication, we report the synthesis, characterization, and electrochemistry of a 2-(2-hydroxyphenyl)-1H-benzimidazole-manganese oxide hybrid. Our results suggest that this compound is a promising model for the manganese cluster together with tyrosine-161 and histidine-190 in photosystem II of plants, algae
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.



Global Trade Item Number

SKUGTIN
194123-5G04061838761064
194123-500G04061838761057
194123-100G04061838761040