DIBUTYLBORON TRIFLUOROMETHANESULFONATE
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- ₹45099
- Product name: DIBUTYLBORON TRIFLUOROMETHANESULFONATE
- CAS: 60669-69-4
- MF: C9H18BF3O3S
- MW: 274.11
- EINECS:
- MDL Number:MFCD00009669
- Synonyms:Dibutylboron trifluoromethanesulfonate, 1M solution in diethylether;dibutylboron triflate solution;TRIFLUOROMETHANESULFONIC ACID ANHYDRIDE WITH DIBUTYLBORINIC ACID);Dibutylboron trifluoromethanesulfonate,98%;Dibutylboryl trifluoromethanesulfonate solution,Dibutylboron triflate solution;Dibutylboron trifluoroMethanesulfonate, 1M solution in diethyl ether, AcroSeal;Dibutylboryl trifluoroMethanesulfonate solution 1.0 M in Methylene chloride;dibutylboranyl trifluoromethanesulfonate
1 prices
Selected condition:
Brand
- ottokemi
Package
- 100mL
- Manufacturerottokemi
- Product number D 1464
- Product descriptionDibutylboryl trifluoromethanesulphonate solution, 1.0 M in methylene chloride
- Packaging100mL
- Price₹45099
- Updated2022-05-26
- Buy
Manufacturer | Product number | Product description | Packaging | Price | Updated | Buy |
---|---|---|---|---|---|---|
ottokemi | D 1464 | Dibutylboryl trifluoromethanesulphonate solution, 1.0 M in methylene chloride | 100mL | ₹45099 | 2022-05-26 | Buy |
Properties
Boiling point :37℃ (0.12 Torr)
Density :1.271 g/mL at 25 °C
Flash point :80 °F
storage temp. :2-8°C
form :Solution
color :Clear light yellow to orange
BRN :1968660
InChIKey :FAVAVMFXAKZTMV-UHFFFAOYSA-N
Density :1.271 g/mL at 25 °C
Flash point :80 °F
storage temp. :2-8°C
form :Solution
color :Clear light yellow to orange
BRN :1968660
InChIKey :FAVAVMFXAKZTMV-UHFFFAOYSA-N
Safety Information
Symbol(GHS): |
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Description
Dibutylboryl trifluoromethanesulfonate may be used in the following studies:- Stereo- and regio-selective synthesis of erythro aldols.
- As a promoter for the solution and polymer-supported trichloroacetimidate-based glycosylations.
- Synthesis of β-alkoxy carbonyl compounds via one-step Mukaiyama aldol-type reaction.
- Aldol-type cyclization for the stereoselective synthesis of cyclic ethers.
- As a reagent for the formation of boron enolates.
- As a complexation aid for the isolation of 1-acyldipyrromethanes.
- As a promoter in [1,2]-Wittig reaction between aldehydes and O-benzyl or O-allyl glycolate esters, creating two contiguous stereocenters (1,2-diol) in good yield without the need for strong base.
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