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550-23-2

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550-23-2 Usage

General Description

2,4,5-tri(furan-2-yl)-4,5-dihydro-1H-imidazole is a chemical compound with a molecular formula of C10H10N2O3. It is a heterocyclic organic compound that contains both imidazole and furan rings. The compound's structure includes three furan groups attached to the imidazole ring, and it is also known as tri(furan-2-yl)imidazole. This chemical is used in various research and industrial applications, including as a building block for the synthesis of new compounds and as a potential pharmaceutical intermediate. Its unique structure and properties make it a valuable component in the development of new materials and drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 550-23-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,5 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 550-23:
(5*5)+(4*5)+(3*0)+(2*2)+(1*3)=52
52 % 10 = 2
So 550-23-2 is a valid CAS Registry Number.

550-23-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,5-tris(furan-2-yl)-4,5-dihydro-1H-imidazole

1.2 Other means of identification

Product number -
Other names 2,4,5-tri-2-furanyl-4,5-dihydro-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:550-23-2 SDS

550-23-2Upstream product

550-23-2Downstream Products

550-23-2Relevant articles and documents

Selective catalysis for the reductive amination of furfural toward furfurylamine by graphene-co-shelled cobalt nanoparticles

Liu, Jianguo,Ma, Longlong,Zhong, Shurong,Zhuang, Xiuzheng

, p. 271 - 284 (2022/01/19)

Amines with functional groups are widely used in the manufacture of pharmaceuticals, agricultural chemicals, and polymers but most of them are still prepared through petrochemical routes. The sustainable production of amines from renewable resources, such as biomass, is thus necessary. For this reason, we developed an eco-friendly, simplified, and highly effective procedure for the preparation of a non-toxic heterogeneous catalyst based on earth-abundant metals, whose catalytic activity on the reductive amination of furfural or other derivatives (more than 24 examples) proved to be broadly available. More surprisingly, the cobalt-supported catalyst was found to be magnetically recoverable and reusable up to eight times with an excellent catalytic activity; on the other hand, the gram-scale tests catalyzed by the same catalyst exhibited the similar yield of the target products in comparison to its smaller scale, which was comparable to the commercial noble-based catalysts. Further results from a series of analytical technologies involving XRD, XPS, TEM/mapping, and in situ FTIR revealed that the structural features of the catalyst are closely in relation to its catalytic mechanisms. In simple terms, the outer graphitic shell is activated by the electronic interaction as well as the induced charge redistribution, enabling the easy substitution of the –NH2 moiety toward functionalized and structurally diverse molecules, even under very mild industrially viable and scalable conditions. Overall, this newly developed catalyst introduces the synthesis of amines from biomass-derived platforms with satisfactory selectivity and carbon balance, providing cost-effective and sustainable access to the wide applications of reductive amination.

INTRACELLULAR ORGANELLE PEPTIDE TARGETED ENZYME SUBSTRATES

-

, (2015/09/22)

This invention relates to substrates and methods for the visualization of intracellular organelles, such as the lysosome, peroxiosome, nucleus, Endoplasmic Reticulum and Golgi Apparatus, based upon organelle enzyme activity. Such compounds represent a novel combination of chemically distinct enzyme substrates with targeting and detection substrates which are activated by enzyme activity inside target organelles to produce a detectable signal. The organelle targeted enzyme substrates of this invention are designed to provide high fluorescence at lower pH values found in some organelles and can be used for monitoring enzyme activity inside cells at very low concentrations.

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