76162-58-8

Basic information

• Product Name: ethyl 3-(p-methoxyphenyl)isothiazole-5-carboxylate
• Synonyms: ethyl 3-(p-methoxyphenyl)isothiazole-5-carboxylate
• CAS NO: 76162-58-8
• Molecular Weight: 263.317
• Mol File: 76162-58-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: ethyl 3-(p-methoxyphenyl)isothiazole-5-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 3-(p-methoxyphenyl)isothiazole-5-carboxylate(76162-58-8)
• EPA Substance Registry System: ethyl 3-(p-methoxyphenyl)isothiazole-5-carboxylate(76162-58-8)

Safety Data

• Hazardous Substances Data: 76162-58-8(Hazardous Substances Data)

Upstream product

• 623-47-2 propynoic acid ethyl ester 
• 52533-09-2 5-(4-methoxyphenyl)-[1,3,4]oxathiazol-2-one 
• 73501-02-7 5-(p-methoxyphenyl)-2-trichloromethyl-1,3,4-oxathiazole 
• 73501-04-9 5-(p-methoxyphenyl)-2-phenyl-2-trifluoromethyl-1,3,4-oxathiazole 
• 73501-03-8 5-(p-methoxyphenyl)-2,2-bis(trichloromethyl)-1,3,4-oxathiazole 

Downstream Products

• 1204424-56-5 C₂₁H₂₄ClNO₇S 
• 1204424-55-4 3-[4-chloro-3-(4-methoxyphenyl)isothiazol-5-yl]propionic acid 
• 1204424-61-2 Triethyl 2-[4-bromo-3-(4-methoxyphenyl)isothiazol-5-yl]ethanetricarboxylate 
• 1204424-60-1 [4-Bromo-3-(4-methoxyphenyl)isothiazol-5-yl]methanol 
• 1204424-54-3 [4-Chloro-3-(4-methoxyphenyl)isothiazol-5-yl]methanol 
• 1204424-53-2 [3-(4-Methoxyphenyl)isothiazol-5-yl]methanol 
• 82424-95-1 3-(4-anisyl)-5-isothiazolecarboxylic acid 

Relevant articles and documents

NITROGEN-CONTAINING AROMATIC HETEROCYCLYL COMPOUND

The present invention provides a compound having excellent regulating action on blood lipid level. The present invention provides a compound represented by the following general formula (I) or a pharmacologically acceptable salt thereof, etc., wherein A represents a 5-membered nitrogen-containing aromatic heterocyclyl group; R1 represents COOH or the like; each R2 represents an alkyl or the like; each R3 represents an optionally substituted phenyl, an optionally substituted phenylalkyl, or the like; m represents 0, 1, 2, or 3; n represents 0 or 1; each of R4, R5, R6, and R7 represents H, an alkyl, or the like; and B represents an optionally substituted naphthyl, an optionally substituted aromatic heterocyclyl, or a group represented by the following formula (II) wherein each of B1 and B2 represents an optionally substituted phenyl or an optionally substituted aromatic heterocyclyl.

Nitrile Sulphide Formation from the Thermal Fragmentation of 1,3,4-Oxathiazoles: a Retro-1,3-dipolar Cycloaddition

1,3,4-Oxathiazoles, on thermolysis, undergo retro-1,3-dipolar cycloaddition to afford carbonyl compounds and nitrile sulphides, which may be trapped by cycloaddition with alkynes and nitriles.