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pentafluoroethyl pentafluorophenyl ketone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 52447-16-2 Structure
  • Basic information

    1. Product Name: pentafluoroethyl pentafluorophenyl ketone
    2. Synonyms: pentafluoroethyl pentafluorophenyl ketone
    3. CAS NO:52447-16-2
    4. Molecular Formula:
    5. Molecular Weight: 314.082
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 52447-16-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: pentafluoroethyl pentafluorophenyl ketone(CAS DataBase Reference)
    10. NIST Chemistry Reference: pentafluoroethyl pentafluorophenyl ketone(52447-16-2)
    11. EPA Substance Registry System: pentafluoroethyl pentafluorophenyl ketone(52447-16-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 52447-16-2(Hazardous Substances Data)

52447-16-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52447-16-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,4 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 52447-16:
(7*5)+(6*2)+(5*4)+(4*4)+(3*7)+(2*1)+(1*6)=112
112 % 10 = 2
So 52447-16-2 is a valid CAS Registry Number.

52447-16-2Relevant articles and documents

Well-defined CuC2F5 complexes and pentafluoroethylation of acid chlorides

Panferova, Liubov I.,Miloserdov, Fedor M.,Lishchynskyi, Anton,Martínez Belmonte, Marta,Benet-Buchholz, Jordi,Grushin, Vladimir V.

supporting information, p. 5218 - 5222 (2015/04/27)

Four new well-defined CuI complexes bearing a C2F5 ligand have been prepared and fully characterized: [(Ph3P)2CuC2F5] (2), [(bpy)CuC2F5] (3), [(Ph3P)Cu(phen)C2F5] (4), and [(IPr)CuC2F5] (5). X-ray structures of all four have been determined, showing that the C2F5-ligated Cu atom can be di- (5), tri- (2 and 3), and tetracoordinate (4). The mixed phen-PPh3 complex 4 is a highly efficient fluoroalkylating agent for a broad variety of acid chlorides. This high-yielding transformation represents the first general method for the synthesis of RCOC2F5 from the corresponding RCOCl. Four well-defined CuC2F5 complexes have been prepared and fully characterized, with [(phen)Cu(PPh3)C2F5] (phen=1,10-phenanthroline) proving to be a remarkably efficient fluoroalkylating agent for a broad variety of acid chlorides (see scheme). The procedure represents the first general method for the one-step conversion of RCOCl into valuable pentafluoroethyl ketones.

Perfluorinated 1H-indazoles and hydrotris(indazol-1-yl)borates. Supramolecular organization and a new synthetic procedure to form scorpionate ligands

Mu?oz, Bianca K.,Ojo, Wilfried-Solo,Jacob, Kane,Romero, Nuria,Vendier, Laure,Despagnet-Ayoub, Emmanuelle,Etienne, Michel

, p. 2451 - 2461 (2014/06/09)

This paper describes the syntheses and full characterization of perfluorinated 1H-indazoles 2-5 and hydrotris(indazolyl)borate thallium complexes 6-9 that contain linear perfluoroalkyl chains varying from two to six carbon atoms in the 3-position. In the solid state, the perfluorinated 1H-indazoles exhibit supramolecular structures that depend on the length of the perfluoroalkyl chain. A catemer of order 3 is observed for the CF 2CF3 derivative 2 (chiral space group P32), catemers of order 2 are observed for the C3F7 and C 4F9 derivatives 3 (chiral space group P212 121, one type of helix in the unit cell) and 4 (space group P21/n, two types of helices in the unit cell), respectively, and stacks of dimers are observed for the indazole with the longer C 6F13 chain 5 (space group P21/c). The perfluorinated hydrotris(indazolyl)borate thallium complexes 6-9 [TlFn-Tp 4Bo,3Rf] have been obtained by a new reaction based on the reaction of HBBr2 (generated in situ from BBr3 and Et3SiH) with the indazolates of 2-5 followed by cation exchange. The X-ray crystal structure of [TlF33-Tp4Bo,3C 3F7] 7 shows that, in addition to coordination to the three nitrogens, the thallium is buried in a nest of fluorines with seven short intramolecular Tl?F contacts with the pendant perfluoropropyl chains. The potential of these highly fluorinated molecules to act as ligands is highlighted. This journal is the Partner Organisations 2014.

Transformation of perfluorinated benzocycloalkenes and alkylbenzenes to their carbonyl derivatives under the action of CF3COOH/SbF5

Zonov, Yaroslav V.,Karpov, Victor M.,Platonov, Vyacheslav E.

, p. 1058 - 1064 (2008/02/10)

Perfluorinated benzocycloalkenes (benzocyclobutene, indan, tetralin), alkylbenzocycloalkenes and alkylbenzenes react with CF3COOH/SbF5 at 20-50 °C giving the corresponding carbonyl derivatives.

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