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

3034-53-5 - 2-Bromothiazole, 99% - A14838 - Alfa Aesar

A14838 2-Bromothiazole, 99%

Número CAS
3034-53-5
Nombre Alternativo

Tamaño Precio ($) Cantidad Disponibilidad
10g 53,87
25g 125,79
50g 214,93
250g 739,20
Añadir al carrito Añadir al presupuesto al por mayor Ver artículo

2-Bromothiazole, 99%

MDL
MFCD00005316
EINECS
221-229-4

Propiedades químicas

Fórmula
C3H2BrNS
Peso molecular
164.02
Punto de ebullición
171°
Punto de inflamabilidad
63°(145°F)
Densidad
1.836
Índice de refracción
1.5930
Solubilidad
It is insoluble in water.

Aplicaciones

2-Bromothiazole, is intended used for research purpose only. It is also used as Aryl halide which are used to N-arylate 5- and 7-azaindoles. Copper-catalyzed cyanation provides 2-cyanothiazole

Notas

Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from Strong oxidizing agents, Hydrogen bromide gas, nitrogen oxides (NOx), Sulphur oxides.

Referencias documentales

Henri Jean Marie Dou.; Roger Gallo.; Parina Hassanaly.; Jacques Metzger. Behavior and stability of catalysts in bi- and triphase transfer catalysis. J. Org. Chem . 1977, 42, (26), 4275-4276.

AO Pittet .; DE Hruza. Comparative study of flavor properties of thiazole derivatives. Journal of Agricultural and Food Chemistry. 1974, 22, (2), 264-269.

2-Lithiothiazole can be obtained by direct lithiation of thiazole or, more conveniently, by exchange with 2-bromothiazole using n-BuLi: J. Org. Chem., 53, 1748 (1988). It behaves as a valuable formyl anion equivalent, and as such has been applied, mainly by Dondoni's group, in the syntheses of a variety of products; see, e.g.: Tetrahedron Lett., 34, 7319, 7323, 7327 (1993). See also 2-(Trimethyl­silyl)­thiazole, B21903. Reaction of 2-lithiothiazole with nitrones gives ɑ-aminoaldehydes: Tetrahedron Lett., 33, 4221 (1992); stereocontrolled addition to C-galacto-pyranosylnitrone has been used in syntheses of destomic acid, a component of the antibiotics destomycin and hygromycin, and of lincosamine, the sugar component of the anticancer antibiotic lincomycin: Synlett, 78 (1993). For applications of 2-lithiothiazole in the synthesis of the aza-sugar (+)-galactostsin, see: J. Org. Chem., 60, 4749 (1995). The Thiazole Aldehyde Synthesis has been reviewed by Dondoni: Synthesis, 1681 (1998).

Indicaciones de peligro y de precaución del GHS

Indicaciones de peligro (UE): H315-H319-H335-H227

Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation. Combustible liquid.

Indicaciones de precaución: P210-P261-P280-P305+P351+P338-P304+P340-P362-P312-P405-P403+P233-P501a

Keep away from heat/sparks/open flames/hot surfaces. - No smoking. Avoid breathing dust/fume/gas/mist/vapours/spray. Wear protective gloves/protective clothing/eye protection/face protection. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Take off contaminated clothing and wash before reuse. Call a POISON CENTER or doctor/physician if you feel unwell. Store locked up. Store in a well-ventilated place. Keep container tightly closed. Dispose of contents/container in accordance with local/regional/national/international regulations.

Otras referencias

Beilstein
105724
Código de tarifa arancelaria unificado
2934.10
TSCA
Yes

Recomendado

Visto recientemente

Productos químicos

Ciencias de la vida

Metales & materiales

Catalizadores

Análisis y material de laboratorio