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5-(4-methoxyphenyl)furan-2(3H)-one is an organic compound characterized by a furan-2(3H)-one core structure, which features a five-membered furan ring with a carbonyl group at position 2 and a 4-methoxyphenyl substituent at position 5. This molecule is a derivative of furanones, which are known for their diverse range of applications in the chemical industry, including as intermediates in the synthesis of pharmaceuticals, agrochemicals, and fragrances. The 4-methoxyphenyl group imparts unique electronic and steric properties to the molecule, potentially influencing its reactivity and physical characteristics. The compound's structure and properties make it a subject of interest for researchers in organic chemistry and material science.

60112-44-9

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60112-44-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60112-44-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,1 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60112-44:
(7*6)+(6*0)+(5*1)+(4*1)+(3*2)+(2*4)+(1*4)=69
69 % 10 = 9
So 60112-44-9 is a valid CAS Registry Number.

60112-44-9SDS

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 5-(4-methoxyphenyl)furan-2(3H)-one

1.2 Other means of identification

Product number -
Other names -

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

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More Details:60112-44-9 SDS

60112-44-9Relevant academic research and scientific papers

A Piperine-Based Scaffold as a Novel Starting Point to Develop Inhibitors against the Potent Molecular Target OfChtI

Deng, Ming-Fei,Duan, Hong-Xia,Han, Qing,Li, Hui-Lin,Li, Xiang,Wang, Jin-E,Wu, Nan,Yang, Qing,Zhang, Jing-Yu,Zhu, Kai

, (2021/07/26)

The insect chitinase OfChtI from the agricultural pest Ostrinia furnacalis (Asian corn borer) is a promising target for green insecticide design. OfChtI is a critical chitinolytic enzyme for the cuticular chitin degradation at the stage of molting. In thi

THE CONVERSION OF FURANS TO 2(3H)-BUTENOLIDES

Pelter, Andrew,Rowlands, Martin

, p. 1203 - 1206 (2007/10/02)

2-Aryl- and 2-alkylfurans are converted into the corresponding 5-organyl-2(3H)-butenolides by the oxidation of boron derivatives with m-chloroperbenzoic acid.

Some Observations Concerning the Lactonization of 3-Aroylpropionic Acids

Tsolomitis, A.,Sandris, C.

, p. 1545 - 1548 (2007/10/02)

The ease of lactonization og the γ-keto acids ArCOCH2CH2COOH is shown to depend on the nature of the aryl group: the presence of electron-releasing substituents on the aryl group results in a more rapid reaction as compared to the presence of electron-wit

Reactions of some Δβ,γ-Butenolides Having no Exocyclic Double bonds

Hashem, A. I.,Shaban, M. E.,El-Kafrawy, A. F.

, p. 763 - 764 (2007/10/02)

Ring-opening of γ-aryl-Δβ,γ-butenolides (I) takes place in a different manner compared to those having an exocyclic double bond at the α-position.I react with hydrazine hydrate in cold or boiling ethanol to give 6-aryl-4,5-dihydropyridazine-3(2

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