31739-56-7 Usage
Description
2-(1H-PYRROL-1-YL)BENZALDEHYDE, also known as pyrrole-2-carboxaldehyde, is a chemical compound with the formula C11H9NO. It features a benzene ring with a 2-pyrrole substituent and an aldehyde functional group. 2-(1H-PYRROL-1-YL)BENZALDEHYDE is recognized for its versatility in organic synthesis and pharmaceutical research, serving as a key building block for the creation of various biologically active molecules.
Uses
Used in Organic Synthesis:
2-(1H-PYRROL-1-YL)BENZALDEHYDE is used as a versatile building block in organic synthesis for the construction of a wide range of biologically active molecules. Its unique structure allows for the formation of complex organic compounds that can be utilized in various applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-(1H-PYRROL-1-YL)BENZALDEHYDE is employed as a reagent in the preparation of heterocyclic compounds. These heterocyclic compounds have potential applications in drug discovery and manufacturing, contributing to the development of new therapeutic agents.
Used in Antimicrobial and Antifungal Drug Development:
2-(1H-pyrrol-1-yl)benzaldehyde has been investigated for its potential antimicrobial and antifungal properties. This makes it a valuable tool in the development of new drugs and treatments for various infectious diseases, offering a promising avenue for combating resistant strains and expanding treatment options.
Used in Drug Discovery:
2-(1H-PYRROL-1-YL)BENZALDEHYDE's role in the synthesis of heterocyclic compounds positions it as a significant player in drug discovery. The exploration of its properties and potential interactions with biological targets can lead to the identification of new pharmaceutical agents with improved efficacy and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 31739-56-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,7,3 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 31739-56:
(7*3)+(6*1)+(5*7)+(4*3)+(3*9)+(2*5)+(1*6)=117
117 % 10 = 7
So 31739-56-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO/c13-9-10-5-1-2-6-11(10)12-7-3-4-8-12/h1-9H
31739-56-7Relevant articles and documents
NOVEL HETEROARYL COMPOUND, ENANTIOMER, DIASTEREOMER OR PHARMACEUTICALLY ACCEPTABLE SALT THEREOF, AND ANTIVIRAL COMPOSITION CONTAINING SAME AS ACTIVE INGREDIENT
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Paragraph 0870; 0871; 0872, (2020/02/14)
The present invention relates to a novel heteroaryl compound, an enantiomer, a diastereomer or a pharmaceutically acceptable salt thereof, and an antiviral composition comprising the same as an active ingredient. The novel compounds represented by formula (I) or formula (II) according to the present invention are remarkably superior in antiviral activity against an influenza virus, and furthermore, have low cytotoxicity and thus low adverse effects on a human body. Therefore, a pharmaceutical composition containing the same as an active ingredient can be effectively used for the prevention or treatment of diseases caused by an influenza virus infection.
Morita-Baylis-Hillman route to 4H-pyrrolo[1,2-a][1]benzazepine derivatives
Park, Sun Pil,Song, Young Seok,Lee, Kee-Jung
experimental part, p. 4703 - 4708 (2009/10/02)
A simple method for synthesizing substituted 4H-pyrrolo[1,2-a][1]benzazepines using acid-assisted cyclization of the Morita-Baylis-Hillman adducts of 2-(1H-pyrrol-1-yl)benzaldehydes with methyl acrylate or methyl vinyl ketone as a key step has been developed.
Lewis acid catalyzed synthesis of 4-aminopyrrolo[1,2-a]quinolin-5-ol derivatives from 2-(1-pyrrolyl)benzaldehyde and isocyanides
Kobayashi, Kazuhiro,Nakahashi, Ryoji,Takanohashi, Atsushi,Kitamura, Taichi,Morikawa, Osamu,Konishi, Hisatoshi
, p. 624 - 625 (2007/10/03)
Reaction of 2-(1-pyrrolyl)benzaldehyde with isocyanides in the presence of a catalytic amount of boron trifluoride diethyl etherate was followed by treatment with acetic anhydride in pyridine to give the corresponding O-acetyl derivatives of 4-alkyl(or ar