1215100-19-8

Basic information

• Product Name: 4-n-butylphenyl trifluoromethanesulfonate
• Synonyms: 4-n-butylphenyl trifluoromethanesulfonate
• CAS NO: 1215100-19-8
• Molecular Weight: 282.284
• Mol File: 1215100-19-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 4-n-butylphenyl trifluoromethanesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-n-butylphenyl trifluoromethanesulfonate(1215100-19-8)
• EPA Substance Registry System: 4-n-butylphenyl trifluoromethanesulfonate(1215100-19-8)

Safety Data

• Hazardous Substances Data: 1215100-19-8(Hazardous Substances Data)

Upstream product

• 358-23-6 trifluoromethylsulfonic anhydride 
• 1638-22-8 4-n-butylphenol 
• 4426-47-5 butylboronic acid 
• 29540-84-9 4-chlorophenyl trifluoromethanesulfonate 
• 1885-46-7 trifluoromethanesulfonic acid difluoromethyl ether 
• 17763-88-1 1,4-phenylene bis(trifluoromethanesulfonate) 
• 92273-73-9 n-butylzinc bromide 

Downstream Products

• 20651-66-5 3-(n-butyl)fluorobenzene 
• 20651-65-4 4-(n-butyl)fluorobenzene 
• 1393879-88-3 4-(4-butylphenyl)-1-methyl-1H-pyrazole 
• 20651-73-4 4-butylbenzonitrile 
• 1329116-13-3 1-butyl-4-(3-methylbut-2-en-1-yl)benzene 
• 61342-04-9 1-butyl-4-(trifluoromethyl)benzene 
• 1447730-56-4 1-butyl-4-(2-methylbut-3-en-2-yl)benzene 
• 41492-05-1 p-bromobutylbenzene 
• 62449-91-6 1-n-butyl-4-i-butylbenzene 
• 104-51-8 1-butylbenzene 

Relevant articles and documents

Phosphine ligand 2 - alkyl - indole skeleton as well as preparation method and application thereof

The invention discloses a phosphine ligand 2 - alkyl - indole skeleton and a preparation method and application thereof, wherein the structural formula of the phosphine ligand 2 - alkyl - indole skeleton is shown I. , Wherein R. 1 . R2/su

Base-promoted selective O-phosphorylation of aryl triflates with P(O)-H compounds

Compared to previous transition metal-catalyzed C-phosphorylation reactions for constructing C–P bonds, in the absence of transition metal catalysts and ligands, a direct O-phosphorylation of aryl triflates selectively occurred with P(O)-H compounds in the presence of a base via the construction of O–P bonds. This transformation proceeds under simple and mild conditions, and provides a new method for the preparation of valuable organophosphoryl compounds from readily available P(O)-H compounds and triflates.

SYNTHESIS OF DIFLUOROMETHYL ETHERS AND SULFIDES

The synthesis of difluoromethyl ethers and sulfides with a simple, non-ozone- depleting reagent is described. The difluoromethylation of phenols with this reagent occurs at room temperature within minutes with exceptional functional group tolerance. The mild conditions makes possible tandem processes for the conversion of aryl boronic acids, aryl halides and arenes to difluoromethyl ethers. Mechanistic studies support a reaction pathway involving nucleophilic attack of the phenolate to difluorocarbene.