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1H-Imidazole, monobenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18715-52-1

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18715-52-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18715-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,1 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 18715-52:
(7*1)+(6*8)+(5*7)+(4*1)+(3*5)+(2*5)+(1*2)=121
121 % 10 = 1
So 18715-52-1 is a valid CAS Registry Number.

18715-52-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name benzoic acid,1H-imidazole

1.2 Other means of identification

Product number -
Other names imidazolium benzoate

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:18715-52-1 SDS

18715-52-1Downstream Products

18715-52-1Relevant academic research and scientific papers

An imidazole-based organocatalyst designed for bulk polymerization of lactide isomers: Inspiration from Nature

Coulembier, Olivier,Josse, Thomas,Guillerm, Brieuc,Dubois, Philippe,Gerbaux, Pascal

, p. 11695 - 11697,3 (2012)

The design of an imidazole-based salt by enzyme-mimicking allowed controlling the ring-opening polymerization of l- and d-LA monomers in bulk. Kinetic study supports a bifunctional activation process only slightly different from the one occurring in Nature.

Toward a new type of proton conductor based on imidazole and aromatic acids

Zi?ba, Sylwia,Dubis, Alina T.,Gzella, Andrzej K.,?awniczak, Pawe?,Pogorzelec-Glaser, Katarzyna,?apiński, Andrzej

, p. 17152 - 17162 (2019)

A new approach towards achieving proton conducting materials based on aromatic acids and heterocyclic bases was proposed. It can lead to a new material in which all hydrogen bonding interactions are of medium or weak strength and rotations of the base and acid molecules are possible. If the above conditions are met, one can expect a high value of proton conductivity governed by the Grotthuss mechanism. Two salts of imidazole, one with benzoic acid having one carboxylic acid group and another with salicylic acid having a carboxylic and hydroxyl group located in the ortho position, were synthesized. Physical properties of these newly synthesized proton conducting salts were investigated using experimental and theoretical methods. The structures of these salts were studied by X-ray diffraction and 1H and 13C NMR techniques. The intermolecular interactions in the salts were analyzed by DFT calculations, within the QTAiM theory, and by Hirshfeld surface analysis. The π-π interactions, the proton conduction pathways, and the transport mechanism are also discussed.

Reaction of Imidazole and 2-Methylimidazole with Copper(II) Salts and Certain Acids

Il’ina, K. A.,Kozik, V. V.,Skorik, N. A.

, p. 1714 - 1721 (2021/11/24)

Abstract: Composition of biligand compounds Cu(C3H4N2, C4H6N2)x(Formula Presented.)2· nH2O obtained by reaction of aqueous suspensions of prepared poorly so

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