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5-AMINO-2-(4-AMINOPHENYL)BENZOFURAN is a chemical compound belonging to the benzofuran class of organic compounds. It features a benzene ring fused to a furan ring, with an amino group at the 5-position and a 4-aminophenyl group at the 2-position.

84102-58-9

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84102-58-9 Usage

Uses

Used in Research and Industrial Applications:
5-AMINO-2-(4-AMINOPHENYL)BENZOFURAN is used as a building block for the synthesis of other organic compounds, contributing to the development of pharmaceuticals and agrochemicals.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 5-AMINO-2-(4-AMINOPHENYL)BENZOFURAN is utilized as a key component in the creation of potential therapeutic agents.
Used in Agrochemical Development:
Similarly, in agrochemicals, 5-AMINO-2-(4-AMINOPHENYL)BENZOFURAN serves as a precursor for the synthesis of various products designed to protect crops and enhance agricultural yields.
Used in Antibacterial Applications:
5-AMINO-2-(4-AMINOPHENYL)BENZOFURAN has been studied for its anti-staphylococcal properties, making it a candidate for use in applications targeting bacterial infections, particularly those caused by Staphylococcus species.
Used in Anti-biofilm Applications:
Additionally, it has demonstrated potential in disrupting biofilms, which are complex bacterial communities that can be resistant to traditional antibiotics, indicating its use in combating biofilm-related infections.

Check Digit Verification of cas no

The CAS Registry Mumber 84102-58-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,1,0 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 84102-58:
(7*8)+(6*4)+(5*1)+(4*0)+(3*2)+(2*5)+(1*8)=109
109 % 10 = 9
So 84102-58-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H12N2O/c15-11-3-1-9(2-4-11)14-8-10-7-12(16)5-6-13(10)17-14/h1-8H,15-16H2

84102-58-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Amino-2-(4-aminophenyl)benzofuran

1.2 Other means of identification

Product number -
Other names 2-(4-aminophenyl)-1-benzofuran-5-amine

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:84102-58-9 SDS

84102-58-9Relevant academic research and scientific papers

INHIBITORS OF HEPATITIS C VIRUS REPLICATION

-

, (2019/05/15)

The present invention relates to compounds of formula (I) that are useful as hepatitis C virus (HCV) NS5A inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5A activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.

Bisazo-benzofuran compounds, their use as charge carrier generating compounds and intermediates for their preparation

-

, (2008/06/13)

There is provided an electrophotographic photoconductor comprising as a charge carrier generating substance a bisazo compound of the general formula (I): wherein R1and R2are the same or different, each representing a hydrogen atom, a

Syntheses of Biscationic, Trypanocidal 1-Benzofuran Compounds

Dann, Otto,Char, Helmut,Griessmeier, Helmut

, p. 1836 - 1869 (2007/10/02)

2-Phenyl-1-benzofurans with the substituents Br, NO2, CN, and -NH2, -NH-C(=NH)-NH2, -C(=NH)-NH2, in 4',5-position were synthesized. - For arylated formamidine derivatives a simple new preparation was found by reacting amine hydrochlorides with dimethylformamide in the presence of cyanamide. - Based on 5- or 6-cyano-1-benzofuran-2-carboxylates a series of α,ω-bis(1-benzofuran-2-yl) derivatives with cyano-, amidino-, or imidazolinyl groups in 5- or 6-position was prepared.

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