334626
Tin(II) fluoride
99%
Synonym(s):
Difluorostannylene, Stannous fluoride, Tin bifluoride, Tin difluoride
About This Item
Recommended Products
Quality Level
Assay
99%
reaction suitability
core: tin
reagent type: catalyst
density
4.57 g/mL at 25 °C (lit.)
SMILES string
F[SnH2]F
InChI
1S/2FH.Sn/h2*1H;/q;;+2/p-2
InChI key
ANOBYBYXJXCGBS-UHFFFAOYSA-L
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Application
- As an inhibitor of Sn4+ in fabrication of formamidinium tin iodide (FASnI3) perovskite solar cells (PSCs) via SnF2–pyrazine complex formation.
- As a catalyst in glycerol ketalization, Knoevenagel condensation and aldol-type reactions.
- In the synthesis of α, β-epoxy ketone from α, α-dibromoacetophenone and aliphatic and aromatic aldehyde via oxidative addition of carbon-halogen bonds.
- In the stereocontrolled [3 + 3] , [3 + 4], [3 + 5] annulations reactions.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Met. Corr. 1 - Skin Irrit. 2
Storage Class Code
6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
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Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.
Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.
Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.
Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.
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