Dibutylboron trifluoromethanesulfonate

Dibutylboron trifluoromethanesulfonate
Names
	IUPAC name Dibutylboranylium trifluoromethanesulfonate
	Other names Dibutylboron triflate
Identifiers
CAS Number	60669-69-4;
3D model (JSmol)	Interactive image;
Abbreviations	DBBT
ChemSpider	23621624;
ECHA InfoCard	100.124.520
PubChem CID	2724243;
CompTox Dashboard (EPA)	DTXSID20369121 ;
	InChI InChI=1S/C8H18B.CHF3O3S/c1-3-5-7-9-8-6-4-2;2-1(3,4)8(5,6)7/h3-8H2,1-2H3;(H,5,6,7)/q+1;/p-1;
	SMILES [B+](CCCC)CCCC.C(F)(F)(F)S(=O)(=O)[O-];
Properties
Chemical formula	C9H18BF3O3S
Molar mass	274.11 g·mol−1
Hazards
GHS pictograms
GHS Signal word	Danger
GHS hazard statements	H314, H318
GHS precautionary statements	P260, P264, P280, P301+330+331, P303+361+353, P304+340, P305+351+338, P310, P321, P363, P405, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Dibutylboron trifluoromethanesulfonate (also called dibutylboron triflate or DBBT) is a reagent in organic chemistry. Its chemical formula is C₉H₁₈BF₃O₃S. It is used in asymmetric synthesis for example in the formation of boron enolates in the aldol reaction.[1]

References

Organic Syntheses, Coll. Vol. 8, p.339 (1993); Vol. 68, p.83 (1990) Link

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

[1] Organic Syntheses, Coll. Vol. 8, p.339 (1993); Vol. 68, p.83 (1990) Link