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1,3-Bis(3-cyanopropyl)imidazolium chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

813458-73-0

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813458-73-0 Usage

Chemical structure

1,3-Bis(3-cyanopropyl)imidazolium chloride is composed of a cationic imidazolium ring with two 3-cyanopropyl substituents attached to the nitrogen atoms and a chloride anion.

Composition

The compound consists of carbon (C), nitrogen (N), hydrogen (H), and chlorine (Cl) atoms.

Applications

It is commonly used as a catalyst in various chemical reactions, particularly in organic synthesis and material science.

Properties

Known for its strong electrostatic interactions and high stability, making it a valuable tool in promoting desired chemical transformations.

Structural characteristics

Its unique structural characteristics and reactivity make it suitable for a wide range of applications, including in the production of pharmaceuticals, dyes, and other fine chemicals.

Safety concerns

Caution should be exercised when handling 1,3-Bis(3-cyanopropyl)imidazolium chloride, as it may pose health and environmental risks if not properly managed.

Reactivity

The compound's reactivity is attributed to the presence of the imidazolium ring and the 3-cyanopropyl substituents, which can participate in various chemical reactions.

Solubility

The solubility of 1,3-Bis(3-cyanopropyl)imidazolium chloride may vary depending on the solvent used, but it is generally soluble in polar aprotic solvents like dimethyl sulfoxide (DMSO) and dimethylformamide (DMF).

Purity

The purity of the compound can impact its effectiveness as a catalyst, so it is essential to ensure that the compound is of high purity for optimal results in chemical reactions.

Storage

To maintain the stability and effectiveness of 1,3-Bis(3-cyanopropyl)imidazolium chloride, it should be stored in a cool, dry place, away from light and moisture, and in a sealed container to prevent contamination or degradation.

Check Digit Verification of cas no

The CAS Registry Mumber 813458-73-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,3,4,5 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 813458-73:
(8*8)+(7*1)+(6*3)+(5*4)+(4*5)+(3*8)+(2*7)+(1*3)=170
170 % 10 = 0
So 813458-73-0 is a valid CAS Registry Number.

813458-73-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-Bis(3-cyanopropyl)-2,3-dihydro-1H-imidazol-1-ium chloride

1.2 Other means of identification

Product number -
Other names -

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:813458-73-0 SDS

813458-73-0Downstream Products

813458-73-0Relevant articles and documents

Imprinted Naked Pt Nanoparticles on N-Doped Carbon Supports: A Synergistic Effect between Catalyst and Support

Bolzan, Gustavo R.,Abarca, Gabriel,Gon?alves, Wellington D. G.,Matos, Carolina F.,Santos, Marcos J. L.,Dupont, Jairton

, p. 1365 - 1372 (2017/12/26)

A synergistic effect resulting from the interaction of small (2.4–3.1 nm) naked Pt nanoparticles (NPs) imprinted on N-doped carbon supports is evidenced by structural, electronic and electrochemical characterization. The size and distribution of the sputtered Pt NPs are found to be related to the nature of the support because Pt NPs are preferentially located at Ngraphitic sites. In addition, Rutherford backscattering shows that a deeper penetration of the Pt NPs is obtained in the N-doped carbon support with larger pore diameters. The ligand effect of the N-doped carbon supports is found to occur by electron donation from Npyrrolic and Ngraphitic sites to the Pt NPs and the electron acceptor behavior of the C=Npyridinic sites. The carbon matrix acquires a basic characteristic (electron-richer, metallic behavior) capable of interacting with metallic NPs akin to a bimetallic-like system. The imprinted Pt NPs are active catalysts for oxidation, although displaying poor catalytic activity for reduction reactions. The catalyst N-doped carbon supports play an important role in the overall catalytic process, rather than only acting as a simple active phase carrier.

IONIC LIQUIDS BASED ON IMIDAZOLIUM SALTS INCORPORATING A NITRILE FUNCTIONALITY

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Page/Page column 18, (2008/06/13)

Novel chemical compounds of the general formula K+A-, in which K+ is a 5- or 6- membered heterocyclic ring having 1-3 hetereo atoms, which can be independently N, S, or 0; with the proviso that at least one of the hetereo atoms must be a quaternized nitrogen atom having a -R'CN substituent, wherein R' is alkyl (C1 to C12); the heterocyclic ring having up to 4 or 5 substituents independently chosen from the moieties: (i) H; (ii) halogen or (iii) alkyl (C1 to C12) , which is unsubstituted or partially or fully substituted by further groups, preferably F, Cl, N(CnF(2n+1-x)Hx)2, O(CnF(2n+1-x)Hx), S02(CnF(2n+1-x)Hx)2 or CnF(2n+1-x)Hx where 1nF(2n+1-x.)Hx.)2, O(CnF(2n+1-x)Hx), S02(CnF(2n+1-x)Hx)2 or CnF(2n+1-x)Hx where 1- is any anion that provides a salt with a low melting point, below about 100 °C; A- can be halide, BF4- , PF6-, N03-, CH3CO2-, CF3SO3-, (CF3SO2)2N-, (CF3SO2)3C- CF3CO2- or N(CN)2- or [BF3RCN]-. These compounds can be used as industrial solvents, especially as ligands for efficient catalyst recycling.

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