125714-79-6

Basic information

• Product Name: 3-(4-METHOXYPHENOXY)-PROPYL METHANESULF&
• Synonyms: 3-(4-METHOXYPHENOXY)-PROPYL METHANESULF&
• CAS NO: 125714-79-6
• Molecular Formula: C₁₁H₁₆O₅S
• Molecular Weight: 260.30674
• Product Categories: Building Blocks;Chemical Synthesis;Organic Building Blocks;Sulfonates/Sulfinates;Sulfur Compounds
• Mol File: 125714-79-6.mol
• Article Data: 4

Chemical Properties

• Melting Point: 56-58 °C(lit.)
• Appearance: /
• CAS DataBase Reference: 3-(4-METHOXYPHENOXY)-PROPYL METHANESULF&(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-METHOXYPHENOXY)-PROPYL METHANESULF&(125714-79-6)
• EPA Substance Registry System: 3-(4-METHOXYPHENOXY)-PROPYL METHANESULF&(125714-79-6)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 125714-79-6(Hazardous Substances Data)

Upstream product

• 150-76-5 4-methoxy-phenol 
• 124-63-0 methanesulfonyl chloride 
• 118943-21-8 3-(4-methoxyphenoxy)-1-propanol 

Downstream Products

• 20744-04-1 1-(3-fluoropropoxy)-4-methoxybenzene 
• 177904-43-7 1,4-Bis-chloromethyl-2-methoxy-5-(3-{4-[(E)-2-(4-nitro-phenyl)-vinyl]-phenoxy}-propoxy)-benzene 
• 177904-42-6 4-[3-(2,5-Bis-chloromethyl-4-methoxy-phenoxy)-propoxy]-benzaldehyde 
• 3722-76-7 3,4-dihydro-6-methoxy-2H-1-benzopyran 
• 177904-41-5 4-[3-(4-Methoxy-phenoxy)-propoxy]-benzaldehyde 

Relevant articles and documents

Unbalanced-Ion-Pair-Catalyzed Nucleophilic Fluorination Using Potassium Fluoride

An unbalanced ion pair promoter (e.g., tetrabutylammonium sulfate), consisting of a bulky and charge-delocalized cation and a small and charge-localized anion, greatly accelerates nucleophilic fluorinations using easy handling KF. We also successfully converted an inexpensive and commercially available ion-exchange resin to the polymer-supported ion pair promoter (A26–SO42–), which could be reused after filtration. Moreover, A26–SO42– can be used in continuous flow conditions. In our conditions, water is well-tolerated.

Direct functionalization of arenes by primary alcohol sulfonate esters catalyzed by gold(III)

Alkylation of arenes by primary alcohol triflate or methanesulfonate esters can be efficiently catalyzed by AuCl3 with silver triflate. Copyright