Cookies disclaimer

Estoy de acuerdo utilizamos cookies para mejorar la experiencia de navegación del usuario y para estudiar cómo se utiliza nuestro sitio web. si navega por nuestro sitio web, estará aceptando el uso de las cookies en las condiciones establecidas en la presente política de cookies. esta política puede ser actualizada, por lo que le invitamos a revisarla de forma regular

1016-58-6 - 4,5-Dimethoxy-2-nitrobenzyl alcohol, 98% - 6-Nitroveratryl alcohol - L00719 - Alfa Aesar

L00719 4,5-Dimethoxy-2-nitrobenzyl alcohol, 98%

Número CAS
1016-58-6
Nombre Alternativo
6-Nitroveratryl alcohol

Tamaño Precio ($) Cantidad Disponibilidad
5g 69,73
25g 273,98
Añadir al carrito Añadir al presupuesto al por mayor Ver artículo

4,5-Dimethoxy-2-nitrobenzyl alcohol, 98%

MDL
MFCD00014701
EINECS
213-806-4

Propiedades químicas

Fórmula
C9H11NO5
Peso molecular
213.19
Punto de fusión
144-148°
Sensibilidad
Light Sensitive
Solubilidad
Soluble in water.

Aplicaciones

4,5-Dimethoxy-2-nitrobenzyl alcohol, is used as Reagent for the protection of alcohols, etc., as ethers which can be cleaved by photolysis involving intramolecular rearrangement to derivatives of o-nitrosobenzaldehyde, which are readily cleaved by hydrolysis. It is also used as photochemical protecting groups in organic synthesis. It is also used as a pharmaceutical intermediate.

Notas

Light Sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from oxidizing agents. Stable under recommended storage conditions.

Referencias documentales

S Kantevari.; CV Narasimhaji.; HB Mereyala. Bis (4, 5-dimethoxy-2-nitrophenyl) ethylene glycol: a new and efficient photolabile protecting group for aldehydes and ketones. Tetrahedron. 200561,(24) , 5849-5854.

H Zhao.; ES Sterner.; EB Coughlin.; P Theato. o-Nitrobenzyl alcohol derivatives: opportunities in polymer and materials science. Macromolecules. 201245,(4) , 1723-1736.

Reagent for the protection of alcohols, etc., as ethers which can be cleaved by photolysis involving intramolecular rearrangement to derivatives of o-nitrosobenzaldehyde, which are readily cleaved by hydrolysis: J. Am. Chem. Soc., 92, 6333 (1970); J. Org. Chem., 37, 2281, 2285 (1972).

For reviews of photochemical protecting groups in organic synthesis, see: Synthesis, 1 (1980); Org. Photochem., 9, 225 (1987).

Otras referencias

Beilstein
1880093
Código de tarifa arancelaria unificado
2909.30
TSCA
No

Recomendado

Visto recientemente

Productos químicos

Ciencias de la vida

Metales & materiales

Catalizadores

Análisis y material de laboratorio