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12-1430

Sigma-Aldrich

Gold(III) chloride

SAJ special grade (dihydrate), ≥98.5%

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About This Item

Linear Formula:
AuCl3
CAS Number:
13453-07-1
Molecular Weight:
303.33
EC Number:
236-623-1
MDL number:
MFCD00014172
UNSPSC Code:
12352300
PubChem Substance ID:
329749639

grade

SAJ special grade (dihydrate)

assay

≥98.5%

reaction suitability

reagent type: catalyst
core: gold

availability

available only in Japan

SMILES string

Cl[Au](Cl)Cl

InChI

1S/Au.3ClH/h;3*1H/q+3;;;/p-3

InChI key

RJHLTVSLYWWTEF-UHFFFAOYSA-K

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Vanajakshi Gudla et al.
The Journal of organic chemistry, 76(24), 9919-9933 (2011-10-28)
An intramolecular approach to generate compounds containing an arylnaphthalene lignan scaffold in high yields is presented. It involves a sequential intramolecular electrophilic attack of carbonyl on arylalkyne followed by benzannulation catalyzed by gold salt. AuCl(3) in combination with AgSbF(6) works
Zhi-Xiong Ma et al.
Organic letters, 14(22), 5736-5739 (2012-11-06)
An imino-Nazarov cyclization using α-aryl-substituted allenamides is described. This gold(I)-catalyzed cascade is efficient and regioselective in constructing a diverse array of synthetically useful aromatic-ring fused cyclopentenamides. The success in this transformation represents a solution to the challenge in establishing an
Ahmed A Elzatahry et al.
International journal of nanomedicine, 7, 2829-2832 (2012-06-30)
This report concerns nanofiber composites that incorporate N-heterocyclic carbenes and the use of such composites for testing antimicrobial and antifungal activities. The nanofiber composites were produced by electrospinning mixtures of the gold chloride or gold acetate complexes of a bis(imino)acenaphthene
Yuanjing Xiao et al.
Organic letters, 14(17), 4662-4665 (2012-08-25)
The cyclic α-imino gold carbene intermediate B is most likely generated in situ via regioselective nitrene transfer from an azido group to a tethered terminal alkyne in the presence of a gold catalyst and at ambient temperature. This highly electrophilic
Martin A Prusinkiewicz et al.
The Analyst, 137(21), 4934-4942 (2012-08-18)
High spatial resolution methods to assess the physiology of growing cells should permit analysis of fungal biochemical composition. Whole colony methods cannot capture the details of physiology and organism-environment interaction, in part because the structure, function and composition of fungal
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