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1H-Imidazolium, 1,3-bis[(1S)-1-phenylpropyl]-, chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

873685-00-8

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873685-00-8 Usage

Chemical compound

1H-Imidazolium, 1,3-bis[(1S)-1-phenylpropyl]-, chloride is a chemical compound.

Ionic liquid

It is commonly used as an ionic liquid in various applications.

Applications

It is used in catalysis, electrochemistry, and as a solvent for organic synthesis.

Type of imidazolium salt

It is a type of imidazolium salt.

Positively charged imidazolium ion

It consists of a positively charged imidazolium ion.

Chloride ion

It also consists of a chloride ion.

1,3-bis[(1S)-1-phenylpropyl]moiety

It refers to the presence of two 1-phenylpropyl groups on the imidazolium ring.

Stereochemistry

The stereochemistry is specified as (1S), indicating the absolute configuration of the carbon center.

High thermal stability

It is known for its high thermal stability.

Low volatility

It is known for its low volatility.

Stable complexes with anions

It has the ability to form stable complexes with various anions.

Check Digit Verification of cas no

The CAS Registry Mumber 873685-00-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,6,8 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 873685-00:
(8*8)+(7*7)+(6*3)+(5*6)+(4*8)+(3*5)+(2*0)+(1*0)=208
208 % 10 = 8
So 873685-00-8 is a valid CAS Registry Number.

873685-00-8Downstream Products

873685-00-8Relevant academic research and scientific papers

Synthesis, Characterization, and Catalytic Activity of Chiral NHC Platinum(II) Pyridine Dihalide Complexes

Blanc, Aurélien,De Frémont, Pierre,Hatey, Delphine,Pale, Patrick,Pertschi, Romain

supporting information, (2020/03/16)

A series of platinum(II) dihalide pyridine complexes bearing chiral C2-symmetric N-heterocyclic carbene (NHC) ligands [Pt(NHC*)(Py)(Hal)2] was synthesized in a one-pot procedure and characterized by NMR spectroscopy and single crystal X-ray diffraction (SC-XRD). The complexes were tested for the asymmetric cycloisomerization of enynol into bicyclo[3.1.0]hexanone and feature an excellent catalytic activity at room temperature along with a modest enantiomeric induction (up to 39% ee).

Enantioselective copper catalysed 1,4-conjugate addition reactions using chiral N-heterocyclic carbenes

Winn, Caroline L.,Guillen, Frédéric,Pytkowicz, Julien,Roland, Sylvain,Mangeney, Pierre,Alexakis, Alexandre

, p. 5672 - 5695 (2007/10/03)

The preparation of a variety of chiral N-heterocyclic carbene (NHC) precursors is described. The relative merits of imidazolinium salts and silver carbenes as NHC precursors are discussed with respect to their synthesis, stability and performance in the copper catalysed conjugate addition of dialkyl zinc reagents to a variety of Michael acceptors. Enantioselectivities of up to 93% were achieved using as little as 4% of chiral ligand.

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