31189
2-Aminobenzimidazole
PESTANAL®, analytical standard
Synonym(s):
2-Benzimidazolamine
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All Photos(2)
About This Item
Empirical Formula (Hill Notation):
C7H7N3
CAS Number:
Molecular Weight:
133.15
Beilstein:
116525
EC Number:
MDL number:
UNSPSC Code:
41116107
eCl@ss:
32151902
PubChem Substance ID:
NACRES:
NA.24
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grade
analytical standard
Quality Level
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
mp
226-230 °C (lit.)
application(s)
agriculture
environmental
format
neat
SMILES string
Nc1nc2ccccc2[nH]1
InChI
1S/C7H7N3/c8-7-9-5-3-1-2-4-6(5)10-7/h1-4H,(H3,8,9,10)
InChI key
JWYUFVNJZUSCSM-UHFFFAOYSA-N
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Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
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Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Ahmad Shaabani et al.
Combinatorial chemistry & high throughput screening, 9(10), 771-776 (2006-12-16)
Tetraheterocyclic benzimidazo[1,2-a]quinazolin-4(1H)-one and tetrahydro-1,2,4-triazolo[5,1-b]quinazolin-8(4H)-one were synthesized in relatively high yields by the condensation reaction of an aldehyde and a cyclic beta-diketone with 2-aminobenzothiazole, 2-aminobenzimidazole or 3-amino-1,2,4-triazole without using any catalyst under solvent-free conditions.
S Sudha et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 84(1), 184-195 (2011-10-11)
In the present work, we reported a combined experimental and theoretical study on molecular structure, vibrational spectra and HOMO-LUMO analysis of 2-aminobenzimidazole (2-ABD). The FTIR (400-4000 cm(-1)) and FT-Raman spectra (50-3500 cm(-1)) of 2-ABD were recorded. The molecular geometry, harmonic
Zinc fingered: new compounds that thwart gram-positive biofilm formation by sequestering zinc.
Dinty J Musk
Chembiochem : a European journal of chemical biology, 11(6), 758-760 (2010-03-02)
Min Zhong et al.
Bioorganic & medicinal chemistry letters, 19(17), 5158-5161 (2009-08-04)
This Letter describes the discovery and key structure-activity relationship (SAR) of a series of 2-aminobenzimidazoles as potent Aurora kinase inhibitors. 2-Aminobenzimidazole serves as a bioisostere of the biaryl urea residue of SNS-314 (1c), which is a potent Aurora kinase inhibitor
2-Aminobenzimidazole derivatives strongly inhibit and disperse Pseudomonas aeruginosa biofilms.
Reto Frei et al.
Angewandte Chemie (International ed. in English), 51(21), 5226-5229 (2012-04-11)
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