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824-79-3 - p-Toluenesulfinic acid sodium salt, 97% (dry wt.), water <5% - Sodium p-toluenesulfinate - 4-Methylbenzenesulfinic acid sodium salt - A11430 - Alfa Aesar

A11430 p-Toluenesulfinic acid sodium salt, 97% (dry wt.), water <5%

Número CAS
824-79-3
Nombre Alternativo
Sodium p-toluenesulfinate
4-Methylbenzenesulfinic acid sodium salt

Tamaño Precio ($) Cantidad Disponibilidad
25g 11,90
100g 42,50
500g 91,10
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p-Toluenesulfinic acid sodium salt, 97% (dry wt.), water <5%

MDL
MFCD00149640
EINECS
212-538-5

Propiedades químicas

Fórmula
C7H7NaO2S
Peso molecular
178.19
Punto de fusión
>300°
Sensibilidad
Hygroscopic
Solubilidad
Slightly soluble in water.

Aplicaciones

p-Toluenesulfinic acid sodium salt is used as an intermediate for the preparation of pharmaceuticals and dispersal dyes. It acts as a curing agent of grouting material. It is also used as a discharge medium of dyes and pigments. Further, it serves as a chemical intermediate in the production of fluorescent pigments and fabric adhesive. In addition to this, it is used as an electroplating brightening agent and curing agent.

Notas

Incompatible with strong oxidizing agents.

Referencias documentales

Alkylation with reactive halides leads to alkyl sulfones. Alkylation of sulfinates can be carried out in a polyethylene glycol as solvent/catalyst: Bull. Chem. Soc. Jpn., 57, 613 (1984). Reaction with allylic alcohols also gives sulfones: J. Org. Chem., 55, 3274 (1990). For asymmetric sulfonylation of allylic chlorides, catalyzed by a chiral Pd complex, see: Tetrahedron: Asymmetry, 6, 643 (1995).

In the presence of CuI, iodoarenes undergo displacement in DMF to give moderate to good yields of diaryl sulfones: Tetrahedron Lett., 36, 6239 (1995).

For use as a precursor of p-toluenesulfonyldiazomethane, via Mannich reaction with formaldehyde and urethane, nitrosation and cleavage with alumina, see: Org. Synth. Coll., 6, 981 (1988):

Also undergoes free-radical reactions in the presence of Cu(II), activated either thermally or by sonication. For example, addition-cyclization of 5-heteroarylpent-1-enes: Synlett, 763 (1995):

Handa, S.; Fennewald, J. C.; Lipshutz, B. H. Aerobic Oxidation in Nanomicelles of Aryl Alkynes, in Water at Room Temperature. Angew. Chem. Int. Ed. 2014, 126 (13), 3500-3503.

Thanatvarakorn, O.; Nakajima, M.; Prasansuttiporn, T.; Ichinose, S.; Foxton, R. M.; Tagami, J. Effect of smear layer deproteinizing on resin-dentine interface with self-etch adhesive. J. dent. 2014, 42 (3), 298-304.

Otras referencias

Beilstein
4621454
Código de tarifa arancelaria unificado
2930.90
TSCA
Yes
RTECS
XT4725000

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