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17113-31-4

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17113-31-4 Usage

General Description

Furan, 2-(p-methoxyphenyl)-, also known as 2-(4-methoxyphenyl)furan, is a chemical compound with the molecular formula C11H10O2. It is a derivative of furan, a heterocyclic compound with a five-membered ring structure containing four carbon atoms and one oxygen atom. This particular derivative has a p-methoxyphenyl group attached to the furan ring. It is commonly used as a building block in the synthesis of various pharmaceuticals and organic compounds. The compound is also known for its potential biological activities, including anti-inflammatory and analgesic properties. Additionally, it has been used in research as a starting material for the development of new drugs and chemical substances.

Check Digit Verification of cas no

The CAS Registry Mumber 17113-31-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,1 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17113-31:
(7*1)+(6*7)+(5*1)+(4*1)+(3*3)+(2*3)+(1*1)=74
74 % 10 = 4
So 17113-31-4 is a valid CAS Registry Number.

17113-31-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methoxyphenyl)furan

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:17113-31-4 SDS

17113-31-4Relevant articles and documents

Efficient procedure for the preparation of 2-bromofuran and its application in the synthesis of 2-arylfurans

Raheem, Mohammed-Abdul,Nagireddy, Jaipal R.,Durham, Robin,Tam, William

, p. 2138 - 2146 (2010)

A simple, straightforward, and scalable procedure for the preparation of 2-bromofuran using N-bromosuccinimide (NBS) in dimethylformamide (DMF) is reported. The described preparation is conducted on a 20 to 50g scale and does not require extractive workup procedures or chromatographic purifications. To illustrate the synthetic applications of 2-bromofuran, palladium-catalyzed Suzuki coupling reactions of the prepared 2-bromofuran with various aryl boronic acids were investigated, and moderate to good yields of 2-arylfurans were obtained. Copyright Taylor & Francis Group, LLC.

New Nickel-Based Catalytic System with Pincer Pyrrole-Functionalized N-Heterocyclic Carbene as Ligand for Suzuki-Miyaura Cross-Coupling Reactions

Guo, Zhifo,Lei, Xiangyang

supporting information, (2021/09/11)

A new catalytic system with Ni(NO3)2·6H2O as the catalyst and a pincer pyrrole-functionalized N-heterocyclic carbene as the ligand was employed in the Suzuki-Miyaura cross-coupling reactions of aryl iodides with arylboronic acids. With 5 mol% catalyst, the catalytic reactions proceeded at 160 °C, giving coupling products in isolated yields of up to 94% in short reaction times (1-4 h). The system worked efficiently with aryl iodides bearing electron-donating or electron-withdrawing groups and arylboronic acids with electron-donating groups. Steric effects were observed for both aryl iodides and arylboronic acids. It is proposed that the reactions underwent a Ni(I)/Ni(III) catalytic cycle.

Pd Nanoparticles Embedded Into MOF-808: Synthesis, Structural Characteristics, and Catalyst Properties for the Suzuki–Miyaura Coupling Reaction

Li, Tang,Pang, Wan,Wang, Jie,Zhang, Xiaoli,Zhao, Zesheng

, (2021/07/31)

Abstract: A heterogeneous single-site catalyst Pd@MOF-808 was successfully synthesized by water-based, green synthesis procedure. The catalytic experiments exhibited the Pd@MOF-808 promoted efficiently the Suzuki–Miyaura coupling reaction without the assistance of organic phosphine ligands at atmospheric pressure conditions. The catalyst also could be applied in the gram-scale synthesis of industrially anti-inflanmatory analgestic Fenbufen. Graphic Abstract: [Figure not available: see fulltext.]

Fabrication of Graphitic Carbon Nitride-Based Film: An Emerged Highly Efficient Catalyst for Direct C—H Arylation under Solar Light

Chaubey, Surabhi,Yadav, Rajesh K.,Kim, Tae Wu,Yadav, Tara Chand,Kumar, Abhishek,Dwivedi,Pandey,Singh, Atul P.

, p. 633 - 639 (2021/02/12)

Photoredox C—H bond formation can proceed in aerobic environment under solar light and has therefore become attractive. Nowadays, different types of expensive novel metal complexes and nanomaterials have been urbanized as photocatalysts for direct C—H bon

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