261998
Boron trifluoride methyl sulfide complex
95%
Synonym(s):
Dimethyl sulfide-trifluoroborane, Trifluoroborane-methyl sulfide
Sign Into View Organizational & Contract Pricing
All Photos(1)
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
Recommended Products
Quality Level
Assay
95%
form
liquid
reaction suitability
core: boron
reagent type: Lewis acid
reagent type: catalyst
density
1.235 g/mL at 25 °C (lit.)
functional group
thioether
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.
Signal Word
Danger
Hazard Statements
Precautionary 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
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Structural optimization of 2, 5-thiophene amides as highly potent and selective 17?-hydroxysteroid dehydrogenase type 2 inhibitors for the treatment of osteoporosis.
Marchais-Oberwinkler S, et al.
Journal of Medicinal Chemistry, 56(1), 167-181 (2012)
Systematics of BX3 and BX2+ Complexes (X= F, Cl, Br, I) with Neutral Diphosphine and Diarsine Ligands.
Burt J, et al.
Inorganic Chemistry, 55(17), 8852-8864 (2016)
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)
Understanding the Reactivity of Enol Ether Radical Cations: Investigation of Anodic Four-Membered Carbon Ring Formation.
Yamaguchi Y, et al.
The Journal of Organic Chemistry, 78(6), 2626-2638 (2013)
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)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service