246869-15-8

Basic information

• Product Name: 2-(CyclopropylMethoxy)-acetic Acid 1,1-DiMethyl-2-[4-(Methylsulfonyl)phenyl]-2-oxoethyl Ester
• Synonyms: 2-(CyclopropylMethoxy)-acetic Acid 1,1-DiMethyl-2-[4-(Methylsulfonyl)phenyl]-2-oxoethyl Ester
• CAS NO: 246869-15-8
• Molecular Formula: C₁₇H₂₂O₆S
• Molecular Weight: 354.41798
• Product Categories: Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals;Sulfur & Selenium Compounds;Aromatics, Pharmaceuticals, Intermediates & Fine Chemicals, Sulfur & Selenium Compounds
• Mol File: 246869-15-8.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 535.6±48.0 °C(Predicted)
• Appearance: /
• Density: 1.246±0.06 g/cm3(Predicted)
• Solubility: Acetone, Chloroform, Dichloromethane
• CAS DataBase Reference: 2-(CyclopropylMethoxy)-acetic Acid 1,1-DiMethyl-2-[4-(Methylsulfonyl)phenyl]-2-oxoethyl Ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(CyclopropylMethoxy)-acetic Acid 1,1-DiMethyl-2-[4-(Methylsulfonyl)phenyl]-2-oxoethyl Ester(246869-15-8)
• EPA Substance Registry System: 2-(CyclopropylMethoxy)-acetic Acid 1,1-DiMethyl-2-[4-(Methylsulfonyl)phenyl]-2-oxoethyl Ester(246869-15-8)

Safety Data

• Hazardous Substances Data: 246869-15-8(Hazardous Substances Data)

Usage

Chemical Properties

White Solid

Upstream product

• 88324-55-4 2-bromo-2-methyl-1-[4-(methylsulfanyl)phenyl]propan-1-one 
• 100-68-5 methyl-phenyl-thioether 
• 246869-08-9 2-(cyclopropylmethoxy)acetic acid 
• 189955-79-1 2-bromo-2-methyl-1-[4-(methylsulfonyl)phenyl]propan-1-one 
• 53207-58-2 2-methyl-1-(4-(methylthio)phenyl)-propan-1-one 
• 180048-73-1 2-hydroxy-2-methyl-1-(4-(methylsulfonyl)-phenyl)propan-1-one 
• 71867-98-6 2-hydroxy-2-methyl-1-(4-(methylthio)phenyl)-propan-1-one 

Downstream Products

• 189954-96-9 3-(Cyclopropylmethoxy)-5.5-dimethyl-4-(4-(methylsulfonyl)phenyl)-5H-furan-2-one 

Relevant articles and documents

Non-luo kaoxi intermediate preparation method (by machine translation)

The invention relates to a preparation method of the midbody non-luo kaoxi, belongs to the technical field of pharmacy. The invention provides a preparation method includes: a raw material first after the reaction with the acyl chloride reagent, with in addition a raw material in the presence of a reaction, after treatment, to obtain the target product. The method of the invention can be the operability is strong, is beneficial to the industrial production of operation and cost control. (by machine translation)

Firocoxib preparation method

The invention discloses a firocoxib preparation method and relates to the technical field of chemical synthesis, in particular to a novel method for synthesizing firocoxib. The novel method for synthesizing the firocoxib includes subjecting thioanisole serving as a raw material to acylation reaction, bromination reaction, oxidizing reaction, esterification reaction and cyclization reaction sequentially so as to obtain the firocoxib. Compared with a traditional technology, the novel method for synthesizing the firocoxib has the advantages that an aftertreatment process is simple without column chromatography separation, and the method is high in yield, low in cost and suitable for industrial production.