Basic information Reaction Safety Supplier Related

[Bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I),98%

Basic information Reaction Safety Supplier Related

[Bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I),98% Basic information

Product Name:
[Bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I),98%
Synonyms:
  • [Bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I),98%
  • Triphenylphosphinegold(I) bis(trifluoromethanesulfonyl)imidate, min. 98%
  • Triphenylphosphinegold(I) bis(trifluoroMethanesulfonyl)iMidate
  • Triphenylphosphinegld(I)bis(trifluoroMethanesulfonyl)iMidate,Min.98%
  • Triphenylphosphinegold(I) bis(trifluoroMethanesulfonyl)iMidate,98%
  • TRIPHENYLPHOSPHINEGLD(I) BIS(TRIFLUOROMETHANESULFONYL)IMIDATE, MIN. 98%
  • Triphenylphosphinegold(Ⅰ) bis(trifluoromethanesulfonyl)imidate
  • [Bis(trifluoroMethanesulfonyl)iMidate](triphenylphosphine)gold(I)
CAS:
866395-16-6
MF:
C20H16AuF6NO4PS2
MW:
740.4
Product Categories:
  • Au
  • metal-phosphine complex
Mol File:
866395-16-6.mol
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[Bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I),98% Chemical Properties

storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
Dichloromethane
form 
Powder
color 
white to off-white
Sensitive 
air sensitive, light sensitive, store cold
Stability:
Hygroscopic, Light-sensitive, Air-sensitive
InChI
InChI=1S/C18H15P.C2F6NO4S2.Au/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;3-1(4,5)14(10,11)9-15(12,13)2(6,7)8;/h1-15H;;/q;-1;/p+1
InChIKey
ZNCATZOEXBYINU-UHFFFAOYSA-O
SMILES
P(C1C=CC=CC=1)(C1C=CC=CC=1)(C1C=CC=CC=1)[Au+][N-](S(=O)(=O)C(F)(F)F)S(=O)(=O)C(F)(F)F
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Safety Information

HS Code 
71159010
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[Bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I),98% Usage And Synthesis

Reaction

  1. Catalyst promoting the addition of nucleophiles to alleneamides.
  2. Gold- and Bronsted acid-catalyzed cycloisomerization of 1,8-diynyl vinyl acetates to bicycle[2.2.1]hept-2-en-7-ones.
  3. Catalyst used for the synthesis of spiro[piperidine-3,3’-oxindoles].
  4. Catalyst used in the gold(I)-catalyzed Rautenstrauch rearrangement.
  5. Gold-catalyzed π-directed regioselective cyclization of bis(o-alkynyl benzyl alcohols): rapid excess to dihydroisobenzofuran derivatives.
  6. Gold compound used in acid-catalyzed cycloisomerization – synthesis of diverse nitrogen-containing spiro heterocycles.
  7. Gold catalyst used in the domino synthesis of functionalized benzofurans and tetracyclic isochromans via formal carboalkoxylation.


Chemical Properties

Light purple powder

Uses

[Bis(trifluoromethanesulfonyl)imidato](triphenylphosphine)gold(I) is a coordination compound.

[Bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I),98%Supplier

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