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Documentos

31189

Supelco

2-Aminobenzimidazole

PESTANAL®, analytical standard

Sinónimos:

2-Benzimidazolamine

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About This Item

Fórmula empírica (notación de Hill):
C7H7N3
Número de CAS:
934-32-7
Peso molecular:
133.15
Beilstein:
116525
Número CE:
213-280-6
Número MDL:
MFCD00005596
Código UNSPSC:
41116107
eCl@ss:
32151902
ID de la sustancia en PubChem:
329753673
NACRES:
NA.24

grado

analytical standard

Nivel de calidad

100

Línea del producto

PESTANAL®

caducidad

limited shelf life, expiry date on the label

técnicas

HPLC: suitable
gas chromatography (GC): suitable

mp

226-230 °C (lit.)

aplicaciones

agriculture
environmental

formato

neat

cadena SMILES

Nc1nc2ccccc2[nH]1

InChI

1S/C7H7N3/c8-7-9-5-3-1-2-4-6(5)10-7/h1-4H,(H3,8,9,10)

Clave InChI

JWYUFVNJZUSCSM-UHFFFAOYSA-N

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Aplicación

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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Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Información legal

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictogramas

Exclamation mark
GHS07

Palabra de señalización

Warning

Frases de peligro

H302

Clasificaciones de peligro

Acute Tox. 4 Oral

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Equipo de protección personal

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Choose from one of the most recent versions:

Certificados de análisis (COA)

Lot/Batch Number
BCCG2973
BCBT4913
SZBC094XV
SZB7318XV
7318X

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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
Claudio Gnaccarini et al.
Journal of the American Chemical Society, 128(24), 8063-8067 (2006-06-15)
RNA cleaving tris(2-aminobenzimidazoles) have been attached to DNA oligonucleotides via disulfide or amide bonds. The resulting conjugates are effective organocatalytic nucleases showing substrate and site selectivity as well as saturation kinetics. The benzimidazole conjugates also degrade enantiomeric RNA. This observation
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