1483-20-1

Basic information

• Product Name: 5-methoxy-1,3-benzoxathiol-2-one
• Synonyms: 1,3-Benzoxathiol-2-one, 5-methoxy-; 1,3-Benzoxathiol-2-one, 5-methoxy-,
• CAS NO: 1483-20-1
• Molecular Formula: C₈H₆O₃S
• Molecular Weight: 182.1964
• Mol File: 1483-20-1.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 323.9°C at 760 mmHg
• Flash Point: 165.2°C
• Density: 1.406g/cm³
• Vapor Pressure: 0.000254mmHg at 25°C
• Refractive Index: 1.624
• CAS DataBase Reference: 5-methoxy-1,3-benzoxathiol-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 5-methoxy-1,3-benzoxathiol-2-one(1483-20-1)
• EPA Substance Registry System: 5-methoxy-1,3-benzoxathiol-2-one(1483-20-1)

Safety Data

• Hazardous Substances Data: 1483-20-1(Hazardous Substances Data)

Upstream product

• 10345-49-0 O-(4-methoxyphenyl) N,N-dimethylcarbamothioate 
• 150-76-5 4-methoxy-phenol 
• 2757-23-5 chloro(chlorosulfanyl)methanone 
• 106-51-4 p-benzoquinone 
• 7735-56-0 5-hydroxybenzo[d][1,3]oxathiol-2-one 
• 74-88-4 methyl iodide 

Downstream Products

• 1616377-41-3 4-(6-methoxybenzo[1,4]oxathiin-2-yl)phenol 
• 1616377-45-7 C₁₅H₁₄O₄S 
• 1483-15-4 2-methanesulfonyl-4-methoxyphenol 
• 1483-18-7 4-methoxy-2-(methylthio)phenol 
• 1483-19-8 2-mercapto-4-methoxyphenol 

Relevant articles and documents

Palladium-catalyzed intramolecular oxidative C-H sulfuration of aryl thiocarbamates

A palladium-catalyzed intramolecular C-H bond sulfuration reaction of aryl thiocarbamates has been developed. This strategy provides a new route to benzo[d][1,3]oxathiol-2-ones with tolerance of a wide range of substituents. Mechanistic studies suggested

NOVEL BENZOXATHIIN DERIVATIVE

Disclosed is a compound represented by the formula (I) below and a pharmaceutically acceptable salt thereof. This compound is useful for treatment of obesity, diabetes and the like. [In the formula (I), Ar represents a benzene ring or the like; X1 represents a nitrogen atom, a sulfur atom or the like; R1 represents an aryl group or the like; X2 represents a group represented by the following formula (II): (wherein R4 and R5 respectively represent a lower alkyl group or the like, and m represents a number of 2-4) or the like; one of X and Y represents an oxygen atom and the other represents a sulfanyl group or the like; and X3-X6 respectively represent -CH-, a nitrogen atom or the like.