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2H-Imidazole, 4-methyl-2,2,5-triphenyl- is a complex organic compound with the chemical formula C23H20N2. It is a derivative of imidazole, a heterocyclic aromatic organic compound with the formula C3H4N2. The compound features a 4-methyl group attached to the imidazole ring, and three phenyl groups (C6H5) are attached to the 2, 2, and 5 positions of the imidazole ring. 2H-Imidazole, 4-methyl-2,2,5-triphenyl- is known for its unique chemical properties and potential applications in various fields, such as pharmaceuticals and materials science. Due to its complex structure, it is often used in research to study the interactions between different functional groups and to develop new compounds with specific properties.

143687-53-0

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143687-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143687-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,6,8 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 143687-53:
(8*1)+(7*4)+(6*3)+(5*6)+(4*8)+(3*7)+(2*5)+(1*3)=150
150 % 10 = 0
So 143687-53-0 is a valid CAS Registry Number.

143687-53-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-2,2,5-triphenylimidazole

1.2 Other means of identification

Product number -
Other names 2H-Imidazole,4-methyl-2,2,5-triphenyl

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:143687-53-0 SDS

143687-53-0Downstream Products

143687-53-0Relevant academic research and scientific papers

Copper-catalyzed [2+3]-annulation of N-H imines with vinyl azides: Access to polyaryl 2: H -imidazoles

Zhu, Zhongzhi,Lin, Hanze,Liang, Baihui,Huang, Junjie,Liang, Wanyi,Chen, Lu,Huang, Yubing,Chen, Xiuwen,Li, Yibiao

, p. 5621 - 5624 (2020/06/19)

A practical method for the synthesis of 2H-imidazoles via a [2+3] annulation of N-H imines with vinyl azides using a copper catalyst is developed. In this conversion, environmentally friendly oxygen is used as the sole oxidant and N2 and H2O are the only by-products. The catalytic transformation, operating under mild conditions, is operationally simple and is considered as a readily available catalytic system having good substrate and functional compatibility with high atom-efficiency without the need for additional ligands or additives.

Photochemistry of Azole N-Oxides. Facile Photoisomerisation of 2H-Imidazole N-Oxides to 1,3-Diaza-6-oxabicyclohex-3-enes and Synthesis of a 1,3-Diaza-4,7-dioxatricyclo1,603,5>heptane

Gainsford, Graeme J.,Woolhouse, Anthony D.

, p. 803 - 809 (2007/10/02)

Ultraviolet irradiation of a series of 2H-imidazole N-oxides 2 has been shown to effect a clean isomerization to derivatives of the new ring system, 1,3-diaza-6-oxabicyclohex-3-ene, 7.Epoxidation of a representative 7 has given access to the hither

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