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2-methoxyphenyl(triphenylphosphine)gold(I) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1243985-65-0

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1243985-65-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1243985-65-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,3,9,8 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1243985-65:
(9*1)+(8*2)+(7*4)+(6*3)+(5*9)+(4*8)+(3*5)+(2*6)+(1*5)=180
180 % 10 = 0
So 1243985-65-0 is a valid CAS Registry Number.

1243985-65-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methoxyphenyl(triphenylphosphine)gold(I)

1.2 Other means of identification

Product number -
Other names .2-methoxyphenyl(triphenylphosphine)gold

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1243985-65-0 SDS

1243985-65-0Relevant academic research and scientific papers

Mild and Efficient Synthesis of Diverse Organo-AuI-L Complexes in Green Solvents

Ingner, Fredric J. L.,Schmitt, Ann-Cathrin,Orthaber, Andreas,Gates, Paul J.,Pilarski, Lukasz T.

, p. 2032 - 2037 (2020/03/11)

An exceptionally mild and efficient method was developed for the preparation of (hetero)aryl-AuI-L complexes using ethanol or water as the reaction medium at room temperature and Ar-B(triol)K boronates as the transmetalation partner. The reaction does not need an exogeneous base or other additives, and quantitative yields can be achieved through a simple filtration as the only required purification method, which obviates considerable waste associated with alternative workup methods. A broad reaction scope was demonstrated with respect to both the L and (hetero)aryl ligands on product Au complexes. Despite the polar reaction medium, large polycyclic aromatic hydrocarbon units can be incorporated on the Au complexes in very good to excellent yields. The approach was demonstrated for the chemoselective manipulation of orthogonally protected aryl boronates to afford a new class of N-heterocyclic carbene-Au-aryl complexes. A mechanistic rationale was proposed.

Mechanochemical synthesis of (hetero)aryl Au(i) complexes

Dyrager, Christine,Gates, Paul J.,Giustra, Zachary X.,Ingner, Fredric J. L.,Novosedlik, Sebastian,Orthaber, Andreas,Pilarski, Lukasz T.

supporting information, p. 5648 - 5655 (2020/09/21)

Growing demand for sustainable chemical syntheses casts mechanochemistry in a new light as an environmentally benign alternative to traditional solvent-based methods. Given recent interest in Au(i) complexes for catalytic, materials, and medicinal applications, we developed a mechanochemical protocol to prepare (hetero)aryl Au(i) complexes under green conditions. The procedure reported here uses C-H or C-B activation to afford the corresponding Au(i) complexes in high yields. Our approach bypasses external heating, long reaction times and the use of toxic solvents. We demonstrate that mechanochemical C-H auration can be used on highly functionalised bioactive substrates. Mechanistic aspects of the C-H auration are discussed.

Palladium-catalyzed cross-coupling reactions of organogold(i) phosphanes with allylic electrophiles

Pena-Lopez, Miguel,Ayan-Varela, Miguel,Sarandeses, Luis A.,Sestelo, Jose Perez

, p. 1686 - 1694 (2012/03/22)

Aryl and alkenylgold(i) phosphanes react regioselectively with allylic electrophiles such as cinnamyl and geranyl halides (bromide, chloride and acetates) under palladium catalysis in THF at 80 °C to afford the α-substitution product with moderate to high yields. When the reaction is performed with a chiral enantiopure secondary acetate, the α-substituted cross-coupling product is obtained with complete inversion of the stereochemistry.

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