Sodium 4-Methylbenzenesulfinate Hydrate 对甲苯亚磺酸钠水合物
CAS 207801-20-5 MFCD00149640
化学结构图
SMILES: O.[Na+].CC1=CC=C(C=C1)S([O-])=O
化学属性
| Mol. Formula | 4-CH3C6H4SO2Na · xH2O |
|---|---|
| Mol. Weight | 178.18 (anhydrous basis) |
| Melting Point | >;300 °C(lit.) |
| TSCA | Yes |
别名和识别编码
| Chemical Name | Sodium 4-Methylbenzenesulfinate Hydrate |
|---|---|
| MDL Number | MFCD00149640 |
| CAS Number | 207801-20-5 |
| Synonym | Sodium p-toluenesulfinate 对甲苯亚磺酸钠 水合物 Sodium p-toluenesulfinate4-Methylbenzenesulfinic acid sodium salt 对甲苯亚磺酸 钠盐 水合物 |
| EC Number | 212-538-5 |
| Beilstein Registry Number | 5682448 |
| PubChem Substance ID | 24900150 |
| Chemical Name Translation | 对甲苯亚磺酸钠水合物 |
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分类
- {SNA} Building Blocks, Chemical Synthesis, Organic Building Blocks, Sulfonic/Sulfinic Acid Salts, Sulfur Compounds
相关文献及参考
- 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).
- 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):
- 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):
- In the presence of CuI, iodoarenes undergo displacement in DMF to give moderate to good yields of diaryl sulfones: Tetrahedron Lett., 36, 6239 (1995).
安全信息
GHS Symbol
- P280 Wear protective gloves/protective clothing/eye protection/face protection. 戴防护手套/防护服/眼睛的保护物/面部保护物。
- P305+P351+P338
- H302 Harmful if swallowed 吞食有害
- H312 Harmful in contact with skin 皮肤接触有害
- H319 Causes serious eye irritation 严重刺激眼睛
- R22 Harmful if swallowed 吞咽有害
