Sodium Trifluoromethanesulfinate

Sodium Trifluoromethanesulfinate

Product Introduction

Sodium trifluoromethanesulfinate Basic information
Product Name: Sodium trifluoromethanesulfinate
Synonyms: SODIUM TRIFLUOROMETHANESULPHINATE;SODIUM TRIFLUOROMETHANESULFINATE;TRIFLUOROMETHANESULFINIC ACID SODIUM SALT;Sodium trifluoromethanesulphinate 96%;sodium trifluoromethanesulfinate CF3NaO2S;finate;Trifluoromethanesulphinic acid, sodium salt;Methanesulfinic acid,1,1,1-trifluoro-, sodiuM salt
CAS: 2926-29-6
MF: CH2F3NaO2S
MW: 158.07
EINECS: 423-490-1
Product Categories: bc0001
Mol File: 2926-29-6.mol
Sodium trifluoromethanesulfinate Structure
 
Sodium trifluoromethanesulfinate Chemical Properties
Melting point <325°C
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility Water (Sparingly)
form powder
color white
BRN 3723394
InChIKey KAVUKAXLXGRUCD-UHFFFAOYSA-M
 
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38-36/38
Safety Statements 26-36/37/39
WGK Germany 3
TSCA No
HazardClass IRRITANT
HS Code 29309090
 
MSDS Information
 
 
Sodium trifluoromethanesulfinate Usage And Synthesis
Chemical Properties White to light yellow solid
Uses Efficient sulfinate salt for the trifluoromethylation of various aryls, aryl boronic acids, alkenes, and alkynes.
Uses Sodium Triflinate (Sodium trifluoromethanesulfinate), is a sulfur-containing building block and Fluorination reagents, used in various organic synthesis. It can be used in a new and convenient method for the copper-catalyzed construction of functional sulfonamides in good yields and excellent chemoselectivity.
Solubility in water soluble in H2O, slightly soluble in MeOH, MeCN, and acetone.
Synthesis At first, an aqueous solution was prepared by dissolving 37.5 g of sodium sulfite in 150 g of water. Then, a metal pressure-proof reactor was charged with this aqueous solution. After that, the atmosphere of the reactor was removed to obtain a reduced pressure. 10.7 g of trifluoromethanesulfonic fluoride was added to the reactor, stirring at 5° C. for 4 hr. The resulting reaction liquid was neutralized with sodium carbonate, followed by water removal. Then, methanol was added to the remaining solid matter to extract the target product. The resulting methanol solution was concentrated to dryness, thereby obtaining 9.7 g of sodium trifluoromethanesulfinate (yield: 88%).
Sodium trifluoromethanesulfinate
 
Sodium trifluoromethanesulfinate Preparation Products And Raw materials
Preparation Products 4-Methylbenzotrifluoride-->3-Trifluoromethylpyridine-->1,4-Bis(trifluoromethyl)-benzene-->2-Amino-5-bromobenzotrifluoride-->4-(TRIFLUOROMETHYL)DIPHENYL ETHER-->2-ETHOXYCARBONYLPHENYL ISOTHIOCYANATE-->1-Fluoropyridinium triflate-->2,5-Dichlorobenzotrifluoride-->4-(TRIFLUOROMETHYLTHIO)BENZOIC ACID-->4-(TRIFLUOROMETHYLTHIO)BROMOBENZENE-->4-NITRO-2-(TRIFLUOROMETHYL)ACETANILIDE-->4-(TRIFLUOROMETHYL)PHENYL ISOTHIOCYANATE-->3-METHYLBENZOTRIFLUORIDE-->Pyrimidine, 2-chloro-5-(trifluoromethyl)- (9CI)-->1,4-PHENYLENE DIISOTHIOCYANATE

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