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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%

Numéro CAS
824-79-3
Synonymes
Sodium p-toluenesulfinate
4-Methylbenzenesulfinic acid sodium salt

Dimensions Prix ($) Quantité Disponibilité
25g 20,61
100g 37,17
500g 91,05
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p-Toluenesulfinic acid sodium salt, 97% (dry wt.), water <5%

MDL
MFCD00149640
EINECS
212-538-5

Propriétés chimiques

Formule
C7H7NaO2S
Poids formulaire
178.19
Point de fusion
>300°
Sensibilité
Hygroscopic
Solubilité
Slightly soluble in water.

Applications

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.

Notes

Incompatible with strong oxidizing agents.

Références bibliographiques

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.

Autres références

Beilstein
4621454
Code tarifaire harmonisé
2930.90
TSCA
Yes
RTECS
XT4725000

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Catalyseurs

Analytique et matériel de laboratoire