Molecular structure of Gold(III) chloride, CAS Number: 13453-07-1
Gold(III) chloride (CAS 13453-07-1)
Alternate Names:
Trichlorogold
CAS Number:
13453-07-1
Molecular Weight:
303.33
Molecular Formula:
AuCl3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Gold(III) chloride nanocrystalline superlattices in gold colloid solution which are prepared by ligand-induction using AuCl3 reduced with sodium borohydride. Gold(III) chloride exhibits limited solubility in water. As a potent oxidizing agent, it finds applications in diverse organic synthesis reactions and serves as a component in the production of gold nanoparticles. Additionally, this compound plays a role in the synthesis of gold-containing compounds and is instrumental in the preparation of catalysts.
Gold(III) chloride (CAS 13453-07-1) References
- Gold(III) chloride catalyzed cyclization of alpha-hydroxyallenes to 2,5-dihydrofurans. | Hoffmann-Röder, A. and Krause, N. 2001. Org Lett. 3: 2537-8. PMID: 11483054
- Gold(III) chloride catalyzed domino processes with isobenzopyrylium cation intermediates. | Dyker, G., et al. 2003. Angew Chem Int Ed Engl. 42: 4399-402. PMID: 14502722
- Mechanisms of gold bioaccumulation by filamentous cyanobacteria from gold(III)-chloride complex. | Lengke, MF., et al. 2006. Environ Sci Technol. 40: 6304-9. PMID: 17120557
- Gold(III) chloride-catalyzed three-component reaction: a facile synthesis of alkynyl derivatives of 1,2-dihydroquinolines and isoquinolines. | Yadav, JS., et al. 2008. J Org Chem. 73: 6857-9. PMID: 18661945
- Gold(III) chloride catalyzed synthesis of 1-cyanoisoindoles. | Heugebaert, TS. and Stevens, CV. 2009. Org Lett. 11: 5018-21. PMID: 19803474
- Gold(III) chloride catalysed synthesis of 5-alkylidene-dihydrothiazoles. | Heugebaert, TS., et al. 2011. Org Biomol Chem. 9: 4791-4. PMID: 21573285
- Gold(III) chloride catalyzed regioselective synthesis of pyrano[3,4-b]indol-1(9H)-ones and evaluation of anticancer potential towards human cervix adenocarcinoma. | Praveen, C., et al. 2011. Bioorg Med Chem Lett. 21: 4170-3. PMID: 21684738
- The golden pathway to thiolate-stabilized nanoparticles: following the formation of gold(I) thiolate from gold(III) chloride. | Barngrover, BM. and Aikens, CM. 2012. J Am Chem Soc. 134: 12590-5. PMID: 22827488
- Reduction of gold(III) chloride to gold(0) on silicate surfaces. | Mohammadnejad, S., et al. 2013. J Colloid Interface Sci. 389: 252-9. PMID: 23044271
- Understanding the microcrystal tests of three related phenethylamines: the ortho-metallated (±)-amphetamine formed with gold(III) chloride, and the tetrachloridoaurate(III) salts of (+)-methamphetamine and (±)-ephedrine. | Wood, MR. and Lalancette, RA. 2013. Acta Crystallogr C. 69: 388-93. PMID: 23579713
- Gold (III) Chloride-Catalyzed 6-endo-trig Oxa-Michael Addition Reactions for Diastereoselective Synthesis of Fused Tetrahydropyranones. | Ciesielski, J., et al. 2013. Adv Synth Catal. 355: 2077-2082. PMID: 24032002
- Molecular Gold Wire from Mixed-Valent Au(I/III) Complexes. | Böge, M. and Heck, J. 2016. Chemistry. 22: 6787-92. PMID: 27032070
- A halogen-free synthesis of gold nanoparticles using gold(III) oxide. | Sashuk, V. and Rogaczewski, K. 2016. J Nanopart Res. 18: 261. PMID: 27642258
Inhibitor of:
AQP12, AQP12A, AQP3, Metallothionein 1G, Nitrate Reductase, and Tesmin.Activator of:
1700065O13Rik, 5730403M16Rik, 6430526N21Rik, C10orf131, Metallothionein 1E, Metallothionein 1F, Metallothionein 1M, Zfp799, and ZNF491.Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Gold(III) chloride, 250 mg | sc-250066 | 250 mg | $55.00 |