15038-67-2

Basic information

• Product Name: o,o'-sulphonylbisphenol
• Synonyms: o,o'-sulphonylbisphenol;2,2'-Sulfonylbisphenol;Einecs 239-113-7;Phenol, 2,2'-sulfonylbis-;Phenol, 2,2'-sulfonyldi-
• CAS NO: 15038-67-2
• Molecular Formula: C₁₂H₁₀O₄S
• Molecular Weight: 250.2704
• EINECS: 239-113-7
• Mol File: 15038-67-2.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 469.7°Cat760mmHg
• Flash Point: 237.9°C
• Appearance: /
• Density: 1.432g/cm³
• CAS DataBase Reference: o,o'-sulphonylbisphenol(CAS DataBase Reference)
• NIST Chemistry Reference: o,o'-sulphonylbisphenol(15038-67-2)
• EPA Substance Registry System: o,o'-sulphonylbisphenol(15038-67-2)

Safety Data

• Hazardous Substances Data: 15038-67-2(Hazardous Substances Data)

Upstream product

• 107775-84-8 bis-(2-methoxy-phenyl)-sulfone 
• 106-41-2 4-bromo-phenol 
• 126770-56-7 1-methoxy-2-[(2-methoxyphenyl)sulfanyl]benzene 
• 53347-31-2 4,4'-dibromo-2,2'-sulfinyl-di-phenol 
• 5336-22-1 5,5'-dibromo-2,2'-dihydroxydiphenyl sulfide 
• 97-24-5 4,4'-dichloro-2,2'-thiodiphenol 
• 950-47-0 phenoxathiin S,S-dioxide 
• 32568-76-6 2,2'-dihydroxydiphenyl sulfoxide 
• 13693-59-9 2,2'-dihydroxyldiphenyl sulfide 

Downstream Products

• 1332638-90-0 2-(1-pyrenylacetyloxy)-2'-hydroxydiphenyl sulfone 
• 583-53-9 2,3-dibromobenzene 

Relevant articles and documents

Li+ selective podand-type fluoroionophore based on a diphenyl sulfoxide derivative bearing two pyrene groups

New podand-type fluoroionophores having two pyrene moieties: 2,2′-bis(1-pyrenylacetyloxy)diphenyl sulfide (3), 2,2-bis(1- pyrenylacetyloxy)diphenyl sulfoxide (4), and 2,2-bis(1-pyrenylacetyloxy) diphenyl sulfone (5), have been synthesized by connecting two 1-pyrenecarbonylmethyl groups with the two hydroxy groups of 2,2-dihydroxydiphenyl sulfide, sulfoxide, and sulfone, respectively. Their complexation behavior toward alkali metal ions was examined by fluorescence spectroscopy. Among these fluoroionophores, compound 4, having a sulfinyl group, showed high selectivity toward Li+.

Carbonates of acetylenic alcohols

Polymerizable carbonate compounds of the formula: wherein A is an aromatic polycycle, R1 and R2 are independently hydrogen atom or alkyl, and n is 1, 2 or 3, are disclosed. They are useful as a component of nonemanating, self-curing and heat resistant resin compositions.