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2-(2-OXO-2H-CHROMEN-3-YL)ACETIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20862-58-2

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20862-58-2 Usage

Derivative of chromen-3-one

The compound is derived from the parent molecule chromen-3-one, which is a heterocyclic aromatic compound.

Contains a carboxylic acid group

The compound has a functional group of carboxylic acid (-COOH) attached to a phenyl ring.

Used in organic synthesis and medicinal chemistry research

The compound is often used as a building block for the synthesis of various biologically active molecules.

Potential anti-inflammatory and analgesic properties

The compound has shown potential in reducing inflammation and pain, making it a subject of interest for drug development.

Applications in the development of dyes and pigments

Due to its chromophoric nature, the compound may have potential applications in the development of dyes and pigments.

Check Digit Verification of cas no

The CAS Registry Mumber 20862-58-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,6 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 20862-58:
(7*2)+(6*0)+(5*8)+(4*6)+(3*2)+(2*5)+(1*8)=102
102 % 10 = 2
So 20862-58-2 is a valid CAS Registry Number.

20862-58-2SDS

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-(2-oxochromen-3-yl)acetic acid

1.2 Other means of identification

Product number -
Other names 3-coumarinylacetic acid

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:20862-58-2 SDS

20862-58-2Relevant academic research and scientific papers

Synthesis of novel coumarin derivatives and in vitro biological evaluation as potential ptp 1b inhibitors

Sun, Cheng,Peng, Chune,Wang, Jian,Wang, Quan,Liu, Wei,Zhou, Honggang,Yang, Cheng

, p. 1711 - 1726 (2013/09/12)

The aim of protein tyrosine phosphatase 1B (PTP 1B) inhibitors is to develop effective drug for diabetes and obesity. Coumarin becomes as a good skeleton, and is often applied in drug design and synthesis. In this paper, we have synthesized a series of novel coumarin derivatives to be as potential PTP 1B inhibitors. The inhibition rate of compound 9 was more than 80%, and the IC50 value was 49.2 μM, which would be considered for further study.

Microwave assisted one pot synthesis of 7-substituted 2-(2-oxo-2H-chromen-3-yl)acetic acids as precursors of new anti-tumour compounds

Kovacova, Silvia,Kovacikova, Lucia,Lacova, Margita,Bohac, Andrej,Salisova, Marta

experimental part, p. 806 - 811 (2011/11/06)

Perkin condensation with subsequent intramolecular lactonisation as one pot syntheses of 2-(2-oxo-2H-chromen-3-yl)acetic acids VIIa-Xa has been studied. The required acids VIIa-Xa were prepared as precursors of recently discovered compounds possessing antineoplastic activities. Syntheses of VIIa-Xa were carried out using para substituted 2-hydroxybenzaldehydes II-VI, succinic acid anhydride, sodium succinate under thermal or microwave conditions. Significant shortening of the reaction time under microwave irradiation was observed (18-50 min instead of 1.5-5 h of heating). Microwave assisted reactions proceeded more smoothly to give higher yield of the required products VIIa-Xa (31-61 %) compared to those under classical thermal conditions e.g. 21.8 % for IXa (Hurenkamp et al., 2007). Seven reaction by-products were isolated and determined as 2H,2′H-3,3′-bichromene-2,2′-diones VIIb-Xb and (E)-3-(2-hydroxystyryl)-2H-chromen-2-ones VIIc-IXc.

Synthesis and photoinduced fluorescence of 3-(2-hetarylethenyl)chromen-2- ones

Bochkov,Yarovenko,Krayushkin,Chibisova,Valova,Barachevskii,Traven',Beletskaya

experimental part, p. 595 - 601 (2009/04/11)

3-(2-Hetarylethenyl)chromen-2-ones were synthesized for the first time, following two different schemes, and their spectral and photochemical properties were studied. The title compounds were found to undergo both reversible and irreversible photoinduced

Snythesis of 3-Styrylcoumarins from Coumarin-3-acetic Acids and 3-Phenacylcoumarins

Chodankar, N. K.,Joshi, S. D.,Sequeria, S.,Seshadri, S.

, p. 427 - 430 (2007/10/02)

The hitherto unknown 3-styrylcoumarin system has been synthesised by two routes.In the first approach, coumarin-3-acetic acids are reacted with aromatic aldehydes to yield directly the 3-styrylcoumarins.The synthesis is limited by the difficulty in obtaining coumarin-3-acetic acids in good yields.The second approach utilises 3-phenacylcoumarins which are reduced to the carbinols and subsequently dehydrated to the corresponding 3-styrylcoumarins.The fluorescence of these compounds and their application to polyester fibre have been studied.

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