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3794-64-7

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3794-64-7 Usage

Description

Silver heptafluorobutyrate, a chemical compound with the formula Ag(CF3CF2CF2CF2COO), is composed of a silver ion (Ag+) and the heptafluorobutyrate anion (CF3CF2CF2CF2COO-). It is a highly reactive and potent compound widely used in various chemical reactions and industries. Due to its potential toxicity and environmental impacts, it should be handled with caution.

Uses

Used in Organic Synthesis:
Silver heptafluorobutyrate is used as a catalyst in organic synthesis for various reactions, such as the activation of carbon-hydrogen bonds and the formation of carbon-carbon bonds. Its high reactivity and selectivity make it a valuable tool in the synthesis of complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, silver heptafluorobutyrate is utilized in the synthesis of various drugs. Its catalytic properties enable the formation of specific chemical bonds and the production of desired pharmaceutical compounds.
Used in Agrochemical Production:
Silver heptafluorobutyrate is employed in the synthesis of agrochemicals, such as pesticides and herbicides. Its ability to catalyze specific reactions contributes to the production of effective and targeted agrochemicals.
Used in Polymer Production:
In the polymer industry, silver heptafluorobutyrate is used as a catalyst for the synthesis of various polymers. Its reactivity and selectivity facilitate the formation of specific polymer structures with desired properties.

Check Digit Verification of cas no

The CAS Registry Mumber 3794-64-7 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 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3794-64:
(6*3)+(5*7)+(4*9)+(3*4)+(2*6)+(1*4)=117
117 % 10 = 7
So 3794-64-7 is a valid CAS Registry Number.
InChI:InChI=1/C4HF7O2.Ag/c5-2(6,1(12)13)3(7,8)4(9,10)11;/h(H,12,13);

3794-64-7 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (L16853)  Silver heptafluorobutyrate, 97%   

  • 3794-64-7

  • 5g

  • 347.0CNY

  • Detail
  • Alfa Aesar

  • (L16853)  Silver heptafluorobutyrate, 97%   

  • 3794-64-7

  • 25g

  • 932.0CNY

  • Detail
  • Aldrich

  • (307424)  Silverheptafluorobutyrate  97%

  • 3794-64-7

  • 307424-5G

  • 347.49CNY

  • Detail

3794-64-7Relevant articles and documents

The Mass Spectra of Some Silver Salts

Roberts, Gerald D.,White V, Edward

, p. 546 - 550 (1981)

Fifteen of twenty-four silver(I) carboxylates examined give useful electron impact mass spectra.The compounds vaporize at moderate temperatures, apparently mainly as dimer with traces of higher oligomer in only a few cases.The molecular ion for the dimer is generally weak or absent, with the most abundant silver containing ion being + in most cases.Metastable defocusing and deuterium labeling experiments on silver acetate have established some of the fragmentation pathways.The reported loss of carbon dioxide from perfluorocarboxylates to give intense peaks for organosilver ions was not observed in this study.Attempts to obtain spectra on the silver salts of organic materials other than carboxylic acids were successful in several cases.Silver trifluoromethanesulfonate, although much less volatile, gives a spectrum and fragmentation very much like the carboxylates, whereas silver trifluoromethanethiolate gives a complex spectrum which suggests tetramer as a major gas phase species.Of three compounds examined which have silver to nitrogen bonding only silver(II) phthalocyanine is sufficiently volatile to give a spectrum without decomposition.The field desorption spectra of the four compounds examined all show the ions AgnXn-1 for X=acetate (n=1-6), X=p-chlorobenzoate (n=1-4), X=methanesulfonate (n=1-7) and X=p-toluenesulfonate (n=1-5).

Aerosol-assisted chemical vapour deposition (AACVD) of silver films from triorganophosphine adducts of silver carboxylates, including the structure of [Ag(O2CC3F7)(PPh3)2]

Edwards, Dennis A,Harker, Robert M,Mahon, Mary F,Molloy, Kieran C

, p. 134 - 146 (2008/10/08)

Silver carboxylates [Ag(O2CR): R = Me, tBu, 2,4,6-Me3C6H2], fluorocarboxlyates [Ag(O2CRf): rf = c3f7, C6F13, C7F15] and their phosphine adducts [Ag(O2CR)·nPR3′: r = me, tBu, 2,4,6-Me3C6H2, R′ = Me, Ph, n = 2; R = Me, R′ = Me, n = 3; Ag(O2CRf).2PPh3, Rf = C3F7, C6F13, C7F15] have been synthesised, characterised spectroscopically and used as precursors in the aerosol-assisted chemical vapour deposition of silver films. All the phosphine adducts produced films, though in general PMe3 adducts, proved more successful than PPh3 analogues. The fluoro-carboxylates and their PPh3 adducts all generated silver films, though the growth rate for the adducts was lower. All these latter films showed carbon impurities while fluorine was also evident in most cases. The X-ray structure of AgO2CC3F7·2PPh3 is also reported.

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