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Sigma-Aldrich

Boron trifluoride methyl sulfide complex

95%

Synonym(s):

Dimethyl sulfide-trifluoroborane, Trifluoroborane-methyl sulfide

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About This Item

Linear Formula:
(CH3)2S · BF3
CAS Number:
Molecular Weight:
129.94
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22

Assay

95%

form

liquid

reaction suitability

core: boron
reagent type: Lewis acid
reagent type: catalyst

density

1.235 g/mL at 25 °C (lit.)

SMILES string

C[S+](C)[B-](F)(F)F

InChI

1S/C2H6BF3S/c1-7(2)3(4,5)6/h1-2H3

InChI key

VPECYQXBNOAJIF-UHFFFAOYSA-N

Application

Boron trifluoride methyl sulfide complex is a common reagent used for dealkylation of ethers. It can also be used to synthesize boron trifluoride complex with phosphine ligands.

Pictograms

FlameCorrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

3.2 °F - closed cup

Flash Point(C)

-16 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Systematics of BX3 and BX2+ Complexes (X= F, Cl, Br, I) with Neutral Diphosphine and Diarsine Ligands.
Burt J, et al.
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Koufaki M
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Understanding the Reactivity of Enol Ether Radical Cations: Investigation of Anodic Four-Membered Carbon Ring Formation.
Yamaguchi Y, et al.
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Novel selective estrogen receptor downregulators (SERDs) developed against treatment-resistant breast cancer.
Xiong R, et al.
Journal of Medicinal Chemistry, 60(4), 1325-1342 (2017)
Experimental and computational exploration of the dynamic behavior of (PNP) BF 2, a boron compound supported by an amido/bis (phosphine) pincer ligand.
DeMott JC
Dalton Transactions, 40(43), 11562-11570 (2011)

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