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

74199-29-4

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74199-29-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74199-29-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,1,9 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 74199-29:
(7*7)+(6*4)+(5*1)+(4*9)+(3*9)+(2*2)+(1*9)=154
154 % 10 = 4
So 74199-29-4 is a valid CAS Registry Number.

74199-29-4SDS

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 1-(1-phenylvinyl)-1H-imidazole

1.2 Other means of identification

Product number -
Other names 1-(1-phenyl-vinyl)-1H-imidazole

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:74199-29-4 SDS

74199-29-4Downstream Products

74199-29-4Relevant academic research and scientific papers

Synthesis of Terminal N-Vinylazoles from Aromatic Aldehydes, DMSO, and Azoles Based DMSO as Terminal Carbon Synthon

Nie, Zhiwen,Lv, Huifang,Li, Hui,Su, Miaodong,Yang, Tonglin,Luo, Weiping,Liu, Qiang,Guo, Cancheng

, p. 4621 - 4626 (2021/09/02)

A protocol for the synthesis of terminal N-vinylazoles from aromatic aldehydes, DMSO, and azoles has been reported. In this strategy, DMSO was involved in the construction of the C=C bond as a terminal carbon synthon. Both aromatic aldehydes and azoles could be well tolerated and give the corresponding terminal N-vinylazoles in 52–91% yields. Based on preliminary experiments, a plausible mechanism is proposed. (Figure presented.).

A general copper-catalyzed coupling of azoles with vinyl bromides

Liao, Qian,Wang, Yuxing,Zhang, Liyun,Xi, Chanjuan

scheme or table, p. 6371 - 6373 (2009/12/08)

(Chemical Equation Presented) A copper-catalyzed methodology for the coupling of vinyl bromides with azoles has been developed. This protocol uses a combination of 10 mol % of copper iodide and 20 mol % of ethylenediamine as catalyst. The reaction proceed

A polymer-bound oxidovanadium(IV) complex prepared from an L-cysteine-derived ligand for the oxidative amination of styrene

Maurya, Mannar R.,Kumar,Correia, Isabel,Adao, Pedro,Pessoa, Joao Costa

, p. 577 - 587 (2008/12/22)

The ligand H2sal-cys (I) derived from salicylaldehyde and Lcysteine has been covalently bonded to chloromethylated polystyrene cross-linked with 5% divinylbenzene. Upon treatment with [VO(acac)2] in dimethylformamide (DMF) the polystyrene-bound ligand PS-H2sal-cys (II) gave the oxidovanadium(IV) complex, PS-[VO(sal-cys)·DMF] (1). The corresponding neat complex, [VO(sal-eta)]2 (2), has also been prepared similarly in methanol. These complexes have been characterised by IR, electronic, EPR spectroscopic studies, magnetic susceptibility measurements and thermal as well as scanning electron micrographs studies. Complex [VO-(sal-eta)]2 exhibits a medium intensity band at 980 cm -1 in the IR spectrum due to ν(V=O) stretch. Broad features of the EPR spectrum for the neat complex along with magnetic susceptibility studies suggest the presence of antiferromagnetic exchange interaction between two vanadium centers in close proximity. Both complexes catalyze the oxidative amination of styrene, in mild basic conditions, with secondary amines (diethylamine, imidazole, and benzimidazole) and gave a mixture of two aminated products in good yields. Amongst the two aminated products, the anti-Markovnikov product is favored over the Markovnikov one due to the steric hindrance posed by the secondary amines. The polymeranchored heterogeneous catalyst is free from leaching during catalytic action and recyclable. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

Synthesis and Antifungal Activity of New 1-Vinylimidazoles

Ogata, Masaru,Matsumoto, Hiroshi,Shimizu, Sumio,Kida, Shiro,Shiro, Motoo,Tawara, Katsuya

, p. 1348 - 1354 (2007/10/02)

Carbonyl compounds I were subjected to an imidazole transfer reaction with N,N'-sulfinyldiimidazole or N,N'-carbonyldiimidazole to obtain the diimidazole II and the monoimidazole III.Various 1-vinylimidazoles IV, derived from o-hydroxyacetophenones by imi

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