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chloro[2-(dicyclohexylphosphino)-3,6-dimethoxy-2',4',6'-triisopropyl-1,1'-biphenyl]gold (I) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1334547-75-9

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1334547-75-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1334547-75-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,4,5,4 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1334547-75:
(9*1)+(8*3)+(7*3)+(6*4)+(5*5)+(4*4)+(3*7)+(2*7)+(1*5)=159
159 % 10 = 9
So 1334547-75-9 is a valid CAS Registry Number.

1334547-75-9 Well-known Company Product Price

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  • Aldrich

  • (763225)  Chloro[2-(dicyclohexylphosphino)-3,6-dimethoxy-2′,4′,6′-triisopropyl-1,1′-biphenyl]gold(I)  97%

  • 1334547-75-9

  • 763225-250MG

  • 1,069.38CNY

  • Detail
  • Aldrich

  • (763225)  Chloro[2-(dicyclohexylphosphino)-3,6-dimethoxy-2′,4′,6′-triisopropyl-1,1′-biphenyl]gold(I)  97%

  • 1334547-75-9

  • 763225-1G

  • 2,806.83CNY

  • Detail

1334547-75-9Relevant academic research and scientific papers

Synthesis, Reactivity, and Bonding of Gold(I) Fluorido-Phosphine Complexes

Rachor, Simon G.,Müller, Robert,Wittwer, Philipp,Kaupp, Martin,Braun, Thomas

, p. 357 - 367 (2022/01/03)

Gold(I) fluorido complexes with phosphine ligands have been synthesized from their respective iodido precursors. The bonding situation in comparison between complexes bearing phosphines and N-heterocyclic carbenes (NHCs) was explored quantum-chemically, obtaining similar results for both. Calculations of the 19F NMR chemical shifts match the experimental values well, including the approximately 40 ppm low-field shifts for the phosphine complexes compared to the NHC complexes, in spite of similar negative charges on fluorine. The reactivity of the highly water-sensitive gold(I) fluorido complexes was studied, resulting in substitution at the metal using trimethylsilyl reagents. The compounds studied were characterized using NMR as well as X-ray diffraction methods.

Gold-Catalyzed Oxidative Cyclization/Aldol Addition of Homopropargyl Alcohols with Isatins

Cai, Ju,Wang, Xin,Qian, Yu,Qiu, Lihua,Hu, Wenhao,Xu, Xinfang

supporting information, p. 369 - 372 (2019/01/11)

A novel gold-catalyzed oxidative cyclization/aldol addition of homopropargyl alcohols with isatins has been developed that provides an effective access to the 3-hydroxyoxindoles in high yields under mild reaction conditions with high diastereoselectivities. In comparison with disclosed transformations of alkyne oxidations via an α-oxo gold carbene route, this is the first example of an aldol-type interception of an ylide (or its enolate form) intermediate with alkyne as a safe and readily available nondiazo carbene precursor.

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