Welcome to LookChem.com Sign In|Join Free

CAS

  • or

31739-56-7

Post Buying Request

31739-56-7 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

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

31739-56-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-pyrrol-1-ylbenzaldehyde

1.2 Other means of identification

Product number -
Other names 2-pyrrolylbenzaldehyde

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:31739-56-7 SDS

31739-56-7Relevant articles and documents

NOVEL HETEROARYL COMPOUND, ENANTIOMER, DIASTEREOMER OR PHARMACEUTICALLY ACCEPTABLE SALT THEREOF, AND ANTIVIRAL COMPOSITION CONTAINING SAME AS ACTIVE INGREDIENT

-

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

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 31739-56-7