1-Bencilimidazol, + 98 %, Thermo Scientific Chemicals

CAS: 4238-71-5 | C10H10N2 | 158.20 g/mol

Número de catálogo	Cantidad
L00802.14 también denominado L00802-14	25 g

Número de catálogo L00802.14

también denominado L00802-14

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Identificadores químicos

CAS4238-71-5

IUPAC Name1-benzyl-1H-imidazole

Molecular FormulaC10H10N2

InChI KeyKKKDZZRICRFGSD-UHFFFAOYSA-N

SMILESC(N1C=CN=C1)C1=CC=CC=C1

Especificaciones Specification Sheet

Appearance (Color)White to pale cream

Assay (GC)≥98.0%

FormCrystals or powder or crystalline powder or fused solid

1-Benzylimidazole acts as an inducer of various cytochrome P-450 isozymes and inhibitor of thromboxane A2 synthase. 1-Benzylimidazole has been used to prepare cyclodextrin-ionic liquid polymer (βCD-BIMOTs-TDI)

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Aplicaciones
El 1-bencilimidazol actúa como inductor de varias isoenzimas del citocromo P-450 e inhibidor de la sintasa de tromboxano A2 . El 1-bencilimidazol se ha empleado en la preparación de polímero líquido iónico de ciclodextrina (βCD-BIMOTs-TDI)

Solubilidad
Soluble en metanol, acetona, DMSO, etanol, ácidos diluidos (libremente solubles), y tampones de pH>6 (libremente solubles). Insoluble en agua.

Notas
Almacenar en un lugar fresco y seco. Mantener el contenedor cerrado cuando no se utilice. Incompatible con agentes oxidantes.

RUO – Research Use Only

General References:

Claudio Pettinari; Fabio Marchetti; Augusto Cingolani and Stefano Bartolini. Tin(IV) and organotin(IV) complexes containing mono or bidentate N-donor ligands—I. 1-benzylimidazole derivatives.Polyhedron.1996, 15 1263-1276.
M Moreno-Manas; J Bassa; N Llado and R.Pleixats. Lithiation of 1-benzylimidazole. A hypothesis on the regioselectivity of the electrophilic attacks on the lithiated species.Journal of heterocyclic Chemistry.1990, 27 673-678.
Can be lithiated and subsequently alkylated at the benzylic position: Synthesis, 303 (1985).