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
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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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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Christina Mark et al.
Nuclear medicine and biology, 40(2), 295-303 (2012-12-26)
The norepinephrine transporter (NET) is an important target for research in neurology and psychology and is involved in the pathophysiology of many neurodegenerative diseases such as Alzheimer's disease and attention deficient hyperactivity disorder. For visualization of NET abundance and deregulation
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
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