63738-92-1

Basic information

• Product Name: α-acetophenonesulfonic acid sodiuM salt
• Synonyms: α-acetophenonesulfonic acid sodiuM salt;sodium 2-oxo-2-phenylethanesulfonate;Benzeneethanesulfonic acid, β-oxo-, sodium salt (1:1);a-Acetophenonesulfonic acid sodium salt
• CAS NO: 63738-92-1
• Molecular Formula: C₈H₇O₄S*Na
• Molecular Weight: 222.19355
• Mol File: 63738-92-1.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: α-acetophenonesulfonic acid sodiuM salt(CAS DataBase Reference)
• NIST Chemistry Reference: α-acetophenonesulfonic acid sodiuM salt(63738-92-1)
• EPA Substance Registry System: α-acetophenonesulfonic acid sodiuM salt(63738-92-1)

Safety Data

• Hazardous Substances Data: 63738-92-1(Hazardous Substances Data)

Usage

General Description

α-acetophenonesulfonic acid sodium salt is a chemical compound that belongs to the class of acetophenonesulfonic acids. It is a white solid and is commonly used as a reagent in the synthesis of pharmaceuticals and agrochemicals. α-acetophenonesulfonic acid sodiuM salt is an important intermediate in organic synthesis and is also utilized as a catalyst in various chemical reactions. It is known for its ability to act as a good nucleophile and to form stable complexes with transition metals. Furthermore, α-acetophenonesulfonic acid sodium salt is widely employed in the production of dyes, pigments, and fragrances, and it serves as an important building block in the manufacture of various specialty chemicals.

Upstream product

• 98-86-2 acetophenone 
• 598-31-2 1-bromoacetone 
• 7757-83-7 sodium sulfite 
• 70-11-1 α-bromoacetophenone 
• 532-27-4 1-chloroacetophenone 

Downstream Products

• 65-85-0 benzoic acid 

Relevant articles and documents

Asymmetric synthesis of β-hydroxy sulfonic acids by BINAP/Ru-catalyzed hydrogenation

BINAP/Ru(II) complexes catalyze enantioselective hydrogenation of sodium β-keto sulfonates in acidic methanol tinder atmospheric pressure of hydrogen at 50 °C to give the corresponding β-hydroxy sulfonates with up to 97% ee in a quantitative yield. The sense of asymmetric induction is predictable. The low-pressure hydrogenation process allows the hectogram-scale synthesis of a variety of optically active β-hydroxy sulfonates, which attract attention in connection with their functions as surfactants, catalysts, enzyme inhibitors, etc.

New heterocyclic precursors for thermal generation of reactive, electron-rich 1,2-diaza-1,3-butadienes

Figure presented The preparation and thermolysis of new stable heterocyclic precursors of 1,2-diaza-1,3-butadienes is described. The resulting reactive diazadienes are trapped in situ with N-phenyldiazamaleimide. The effect of precursor structure on the temperature at which the diazadienes are generated is discussed.