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Merck

194123

Benzimidazole

98%

Synonyme(s) :

1,3-Benzodiazole, BZI

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A propos de cet article

Formule empirique (notation de Hill) :
C7H6N2
Numéro CAS:
Poids moléculaire :
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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Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Classe de stockage

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