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Silver pentafluorobenzoate is a chemical compound with the formula C7AgF5O2, consisting of a silver ion (Ag+) and a pentafluorobenzoate ion (C7F5O2-). It is a white crystalline solid that is highly sensitive to moisture and air, making it prone to hydrolysis. silver pentafluorobenzoate is primarily used as a reagent in organic synthesis, particularly in the preparation of various fluorinated compounds and as a catalyst in certain chemical reactions. Due to its reactivity, it is essential to handle silver pentafluorobenzoate with care, typically under an inert atmosphere or in a glovebox to prevent unwanted side reactions.

3796-31-4

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3796-31-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3796-31-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,9 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3796-31:
(6*3)+(5*7)+(4*9)+(3*6)+(2*3)+(1*1)=114
114 % 10 = 4
So 3796-31-4 is a valid CAS Registry Number.

3796-31-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name silver pentafluorobenzoate

1.2 Other means of identification

Product number -
Other names Silberpentafluorbenzoat

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3796-31-4 SDS

3796-31-4Upstream product

3796-31-4Relevant academic research and scientific papers

Attempts to prepare mixed diarylgold(III) complexes containing a pentafluorophenyl group. Synthesis of 1N)-(pentafluorophenyl)gold(III) complexes

Vicente, Jose,Bermudez, Maria Dolores,Chicote, Maria Teresa,Sanchez-Santano, Maria Jose

, p. 129 - 136 (1989)

reacts (1/1) with (PhCH2PPh3) to give (PhCH2PPh3) (1) or (Me4N)Au(C6F5)Cl3> (2b), respectively.Complex 1 reacts with chlorine to give (PhCH2PPh3) (2a). reacts with AgOOCC6F5 (1/2) to give (3), which does not undergo decarboxylation when heated as a solid in the range 30-400 deg C.The reaction of with and (Me4N)Cl (2/1/2) affords (4) which reacts with KBr or AgO2CMe to give (X=Br (5), O2CMe (6)) and with pyridine (py) in the presence of NaClO4 to give the cationic species (7).

Dinuclear palladium(II) compounds with bridging cyclometalated phosphines. Synthesis, crystal structure and electrochemical study

Koshevoy, Igor O.,Lahuerta, Pascual,Sanau, Mercedes,Ubeda, M. Angeles,Domenech, Antonio

, p. 5536 - 5541 (2007/10/03)

The structural characterization of bis-cyclometalated palladium(ii) compounds of formula Pd2[(-(C6X4)PPh 2]2(-O2CR)2 [X = H, R = CH 3 (3), CF3 (4), C(CH3)3 (5) and C6F5 (6); X = F, R = CH3 (7) and CF 3(8)], has confirmed its paddle wheel structure with two palladium atoms bridged by two acetates and two metalated phosphines in a head-to-tail arrangement. The Pd...Pd distances are in the range 2.6779(16)-2.7229(8) A. Under cyclic voltammetric conditions, compounds 3-6, in CH 2Cl2 solution, were found to undergo a reversible oxidation peak in the range of potential values 0.84-1.25 V. A second partially-reversible oxidation is observed at more positive potentials (1.37-1.55 V). For compounds 3-5 in the presence of chlorides, the first oxidation becomes a two-electron process presumably leading to a neutral [Pd(iii)-Pd(iii)] species with a metal-metal bond. The Royal Society of Chemistry 2006.

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