4-ベンゼンスルフィン酸ナトリウム(873-55-2)

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4-ベンゼンスルフィン酸ナトリウム 製品概要
化学名:4-ベンゼンスルフィン酸ナトリウム
英語化学名:BENZENESULFINIC ACID SODIUM SALT
别名:4-CHLOROBENZENESULPHINIC ACID SODIUM SALT;4-CHLOROBENZENESULFINIC ACID SODIUM SALT HYDRATE;SODIUM 4-CHLOROBENZENE SULFINIC ACID;P-CHLOROBENZENESULFINIC ACID SODIUM SALT;BENZENESULFINIC ACID NA SALT;Benzenesulfinic acid sodium salt;BENZENSULFINIC ACID SODIUM SALT;Benzenesulfinic acid/Sodium benzene sulphinate
CAS番号:873-55-2
分子式:C6H5NaO2S
分子量:164.16
EINECS:212-842-8
カテゴリ情報:Pharmaceutical Intermediates;Industrial/Fine Chemicals
Mol File:873-55-2.mol
4-ベンゼンスルフィン酸ナトリウム
4-ベンゼンスルフィン酸ナトリウム 物理性質
融点 >300 °C(lit.)
沸点 83-84 °C
比重(密度) 1.45[at 20℃]
貯蔵温度 Inert atmosphere,Room Temperature
溶解性Water
外見 Crystals or Crystalline Powder
White
水溶解度 Soluble in water.
Sensitive Hygroscopic
BRN 3598405
LogP-3.54
CAS データベース873-55-2(CAS DataBase Reference)
EPAの化学物質情報Benzenesulfinic acid, sodium salt (873-55-2)
安全性情報
主な危険性 Xi,Xn
Rフレーズ 36/37/38-20/21/22
Sフレーズ 26-37/39-36-24/25
WGK Germany 1
RTECS 番号DA9135000
TSCA T
HSコード 29309090
MSDS Information
ProviderLanguage
Benzenesulfinic acid sodium salt English
ACROS English
ALFA English
4-ベンゼンスルフィン酸ナトリウム Usage And Synthesis
化学的特性white crystalline powder or crystals
使用Benzenesulfinic acid sodium salt has been used in synthesis of sulfones by reaction of organic halides and sodium benzenesulfinate using higher alcohols or diols as solvents.It was also used in the synthesis of aryl sulfones via copper-catalyzed cross-coupling with boronic acids and vinyl sulfones via reaction with vicinal dibromides.
使用It is used as a polymer adhesive enhancers, plasticizers for plasticized and modified of polyamide, epoxy resin, phenolic resin. It is designed for manufacturing of photography, pharmaceutical, electroplating industry, can be used as photo-reducing agent.
使用Benzenesulfinic Acid Sodium Salt is used reduce the adverse chemical interaction involved in the coupling of self/dual-cured composites to hydrated dentin.
一般的な説明Benzenesulfinic acid sodium salt when treated with alkynylselenonium salts yields (Z)-β-alkoxyvinylsulfones. It undergoes rhodium-catalyzed desulfinative coupling with aldehydes to yield ketones.
純化方法Dissolve it in the minimum volume of O2 free H2O (prepared by bubbling N2 through for 2 hours) and adding O2 free EtOH (prepared as for H2O), set aside at 4o overnight under N2, filter, wash with EtOH, then Et2O and dry in vacuo. The Na salt is relatively stable to air oxidation, but is best kept under N2 in the dark. Also recrystallise it from EtOH and dry it at 120o for 4hours in a vacuum. [Kornblum & Wade J Org Chem 52 5301 1987, Beilstein 11 II 2, 11 IV 3.]
Tags:873-55-2