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About This Item
Linear Formula:
Sn(CH3CO2)2
CAS Number:
Molecular Weight:
236.80
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12161600
EC Number:
211-335-9
MDL number:
Product Name
Tin(II) acetate,
form
solid
Quality Level
reaction suitability
core: tin, reagent type: catalyst
mp
180-182 °C (lit.)
SMILES string
CC(=O)O[SnH2]OC(C)=O
InChI
1S/2C2H4O2.Sn/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+2/p-2
InChI key
PNOXNTGLSKTMQO-UHFFFAOYSA-L
General description
Tin(II) acetate can be used as a photocatalyst to produce Arylstannane(IV) Reagents.
Application
- Enhances the rate of thermal depolymerization of poly(lactic acid) fibers
- Reactant for the synthesis of Sn-Cu bimetallic nanoparticles
- used in in preparation of tin anode by organic electroplating for rechargeable thin-film batteries
- Used as tin source for preparation of high surface area tin oxide catalysts
Used to prepare tin(IV) oxide thin films by photochemical vapor deposition. With palladium(II) acetate, an efficient catalytic system for C-H activation of the methoxy group of anisole.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Keiko Yakabi et al.
ChemSusChem, 10(18), 3652-3659 (2017-08-15)
The Baeyer-Villiger oxidation is a key transformation for sustainable chemical synthesis, especially when H
Photocatalytic Reaction of Aryl Halides with Tin (II) Acetate to Generate Arylstannane (IV) Reagents
Zemtsov AA, et al.
ACS Catalysis, 13, 12766-12773 (2023)
The Journal of Organic Chemistry, 59, 7521-7521 (1994)
