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5-(3-Methoxyphenyl)-2-furoic acid is a furoic acid derivative with the molecular formula C12H10O4. It is a white solid that is sparingly soluble in water but more soluble in organic solvents. This chemical compound belongs to a class of organic compounds containing a furoic acid moiety and has potential applications in the pharmaceutical and chemical industries. Its properties make it suitable for use in various synthetic processes and as a building block for more complex molecules. Additionally, it may have potential pharmacological properties, making it an interesting compound for further research and development.

54022-96-7

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54022-96-7 Usage

Uses

Used in Pharmaceutical Industry:
5-(3-Methoxyphenyl)-2-furoic acid is used as a building block for the synthesis of more complex pharmaceutical compounds. Its unique structure and properties make it a valuable component in the development of new drugs with potential therapeutic applications.
Used in Chemical Industry:
In the chemical industry, 5-(3-Methoxyphenyl)-2-furoic acid is used as an intermediate in the synthesis of various organic compounds. Its reactivity and solubility in organic solvents make it a suitable candidate for use in a wide range of chemical reactions.
Used in Research and Development:
5-(3-Methoxyphenyl)-2-furoic acid is used as a research compound for exploring its potential pharmacological properties. Its unique structure and properties make it an interesting compound for further investigation, which may lead to the discovery of new therapeutic agents or applications in the pharmaceutical field.
Used in Drug Synthesis:
5-(3-Methoxyphenyl)-2-furoic acid is used as a key component in the synthesis of drugs with potential therapeutic effects. Its presence in the molecular structure of these drugs may contribute to their pharmacological activity and efficacy.
Used in Organic Synthesis:
In organic synthesis, 5-(3-Methoxyphenyl)-2-furoic acid is used as a versatile building block for the creation of a variety of organic compounds. Its reactivity and solubility in organic solvents make it a valuable component in the synthesis of complex organic molecules for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 54022-96-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,0,2 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 54022-96:
(7*5)+(6*4)+(5*0)+(4*2)+(3*2)+(2*9)+(1*6)=97
97 % 10 = 7
So 54022-96-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H10O4/c1-15-9-4-2-3-8(7-9)10-5-6-11(16-10)12(13)14/h2-7H,1H3,(H,13,14)

54022-96-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(3-methoxyphenyl)furan-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 5-(3-methoxy-phenyl)-furan-2-carboxylic 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:54022-96-7 SDS

54022-96-7Relevant academic research and scientific papers

Synthesis and SAR of 5-aryl-furan-2-carboxamide derivatives as potent urotensin-II receptor antagonists

Lim, Chae Jo,Kim, Nam Hui,Park, Hye Jin,Lee, Byung Ho,Oh, Kwang-Seok,Yi, Kyu Yang

, p. 577 - 580 (2019/01/05)

The synthesis and biological evaluation as potential urotensin-II receptor antagonists of a series of 5-arylfuran-2-carboxamide derivatives 1, bearing a 4-(3-chloro-4-(piperidin-4-yloxy)benzyl)piperazin-1-yl group, are described. The results of a systemat

Discovery of new C3aR ligands. Part 1: Arginine derivatives

Denonne, Frederic,Binet, Sophie,Burton, Maggi,Collart, Philippe,Dipesa, Alan,Ganguly, Tanmoy,Giannaras, Alexander,Kumar, Seema,Lewis, Timothy,Maounis, Florence,Nicolas, Jean-Marie,Mansley, Tamsin,Pasau, Patrick,Preda, Dorin,Stebbins, Karin,Volosov, Alexander,Zou, Dong

, p. 3258 - 3261 (2008/02/08)

The synthesis and in vitro binding of several new arginine-containing C3aR ligands are reported. DMPK properties and functional activities of selected compounds have been evaluated. One compound is shown to be active in an in vivo model of airway inflamma

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