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

108-77-0 - Cyanuric chloride, 98% - TCT - 2,4,6-Trichloro-1,3,5-triazine - L03442 - Alfa Aesar

L03442 Cyanuric chloride, 98%

Número CAS
108-77-0
Nombre Alternativo
TCT
2,4,6-Trichloro-1,3,5-triazine

Tamaño Precio ($) Cantidad Disponibilidad
50g 17,10
250g 20,30
1000g 82,80
Añadir al carrito Añadir al presupuesto al por mayor Ver artículo

Cyanuric chloride, 98%

MDL
MFCD00006046
EINECS
203-614-9

Propiedades químicas

Fórmula
C3Cl3N3
Peso molecular
184.41
Punto de fusión
145-149°
Punto de ebullición
192-194°
Punto de inflamabilidad
>190°(374°F)
Densidad
1.920
Sensibilidad
Moisture Sensitive
Solubilidad
Soluble in acetone, diethyl ether, dioxane, chloroform, carbon tetrachloride and ketones. Slightly soluble in methanol. Insoluble in cold water.

Aplicaciones

Reagent for detection of glycine in presence of other amino acids.Cyanuric chloride is a reagent used for the conversion of alcohols and carboxylic acids to alkyl chlorides and acid chlorides respectively. It acts as an intermediate to prepare dyestuffs, optical brighteners, tanning agents, UV-absorbing agent, softening agents and pharmaceuticals. It is also used as a precursor to dyes and crosslinking agents due to the presence of reactive chlorine atoms. It is used as a dehydrating agent as well as reacting with dimethylformamide to give Gold’s reagent, which is a versatile source of aminoalkylations and a precursor to heterocycles. Further, it is considered as an alternative to oxalyl chloride in the Swern oxidation. In addition to this, it is involved in the synthesis of adenosine receptor ligand.

Notas

Air and moisture sensitive. Store in a cool place. Incompatible with strong oxidizing agents, strong acids, alcohols, dimethylformamide, amines and dimethyl sulfoxide.

Referencias documentales

In the presence of triethylamine, carboxylic acids are converted to their acid chlorides, allowing in situ formation of esters, amides and peptides: Tetrahedron Lett., 20, 3037 (1979). Similarly, sulfonic acids are converted to sulfonyl chlorides: Tetrahedron Lett., 44, 1499 (2003). ω-Hydroxy acids are converted to their lactones: Tetrahedron Lett., 21, 1893 (1980). Mild reagent in ß-lactam synthesis: Synthesis, 209 (1981). Carboxylic acids, including N-Boc, -Fmoc and -Cbz amino acids have been converted to alcohols in good yield by activation with cyanuric chloride and N-methylmorpholine (NMM), followed by reduction with aqueous NaBH4: Tetrahedron Lett., 40, 4395 (1999). Hydroxamic acids can also be prepared in a simple one-flask method using hydroxylamine hydrochloride in the presennce of NMM and DMAP: Org. Lett., 5, 2715 (2003).

Effects deoxygenation of diaryl sulfoxides. Alkyl sulfoxides undergo ɑ-chlorination, which can be avoided by using cyanuric fluoride: Synthesis, 221 (1980).

For use, in combination with DMSO, in a mild and efficient alternative to the Swern oxidation of alcohols to aldehydes or ketones, see: J. Org. Chem., 66, 7907 (2001).

Reagent for dehydration of aldoximes: J. Chem. Soc., Chem. Commun., 1226 (1972), and primary carboxamides: Synthesis, 657 (1980) to nitriles. The Vilsmeier-type complex with DMF also converts aldoximes cleanly to nitriles; ketoximes undergo the Beckmann rearrangement at room temperature in high yield: J. Org. Chem., 67, 6272 (2002). The complex converts primary and secondary alcohols to alkyl chlorides in high yield; addition of NaBr affords mainly the alkyl bromide: Org. Lett., 4, 553 (2002); whereas with 4 eq. of LiF, primary alcohols are selectively formylated, providing a mild and convenient method for their protection: J. Org. Chem., 67, 5152 (2002).

For a brief feature on uses of the reagent in synthesis, see: Synlett, 2156 (2006).

Wang, H.; Li, C.; Wang, W.; Jin, W. J. Strength order and nature of the π-hole bond of cyanuric chloride and 1, 3, 5-triazine with halide. Phys. Chem. Chem. Phys. 2015, 17 (32), 20636-20646.

Anbia, M.; Khoshbooei, S. Functionalized magnetic MCM-48 nanoporous silica by cyanuric chloride for removal of chlorophenol and bromophenol from aqueous media. J. nanostructure chem. 2015, 5 (1), 139-146.

Indicaciones de peligro y de precaución del GHS

Indicaciones de peligro (UE): H302-H330-H314-H317

Harmful if swallowed. Fatal if inhaled. Causes severe skin burns and eye damage. May cause an allergic skin reaction.

Indicaciones de precaución: P303+P361+P353-P304+P340-P305+P351+P338-P320-P405-P501a

IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Specific treatment is urgent (see label). Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.

Otras referencias

Beilstein
124246
Clase de peligro
8
Grupo de embalaje
II
Código de tarifa arancelaria unificado
2933.69
TSCA
Yes
RTECS
XZ1400000

Recomendado

Visto recientemente

Productos químicos

Ciencias de la vida

Metales & materiales

Catalizadores

Análisis y material de laboratorio