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CAS

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83528-03-4

5-Amino-1-benzofuran-2(3H)-one, also known as 5-Aminoindanone or ABF, is an organic compound with the chemical formula C8H7NO2. It is a heterocyclic compound that contains both an amino group and a ketone group, and it is commonly used in the synthesis of pharmaceuticals and other organic compounds. 5-Amino-1-benzofuran-2(3H)-one has been studied for its potential antiviral and antibacterial properties, and it has also been used in the development of fluorescent probes for detecting metal ions and other molecules. 5-Amino-1-benzofuran-2(3H)-one is of interest to researchers and chemists due to its unique structure and potential applications in various fields.

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  • 83528-03-4 Structure

  • Basic information

    1. Product Name: 5-Amino-1-benzofuran-2(3H)-one
    2. Synonyms: 5-Amino-1-benzofuran-2(3H)-one;5-AMinobenzofuran-2(3H)-one
    3. CAS NO:83528-03-4
    4. Molecular Formula: C8H7NO2
    5. Molecular Weight: 149.14668
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83528-03-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 357.168°C at 760 mmHg
    3. Flash Point: 200.772°C
    4. Appearance: /
    5. Density: 1.377g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.656
    8. Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
    9. Solubility: N/A
    10. CAS DataBase Reference: 5-Amino-1-benzofuran-2(3H)-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-Amino-1-benzofuran-2(3H)-one(83528-03-4)
    12. EPA Substance Registry System: 5-Amino-1-benzofuran-2(3H)-one(83528-03-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 83528-03-4(Hazardous Substances Data)

83528-03-4 Usage

Uses

Used in Pharmaceutical Industry:
5-Amino-1-benzofuran-2(3H)-one is used as a key intermediate in the synthesis of various pharmaceuticals for its versatile chemical properties and potential therapeutic effects.
Used in Antiviral and Antibacterial Applications:
5-Amino-1-benzofuran-2(3H)-one is used as an antiviral and antibacterial agent for its potential to inhibit the growth and replication of viruses and bacteria, contributing to the development of new treatments for infectious diseases.
Used in Analytical Chemistry:
5-Amino-1-benzofuran-2(3H)-one is used in the development of fluorescent probes for detecting metal ions and other molecules, enabling researchers to study chemical interactions and monitor environmental conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 83528-03-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,5,2 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 83528-03:
(7*8)+(6*3)+(5*5)+(4*2)+(3*8)+(2*0)+(1*3)=134
134 % 10 = 4
So 83528-03-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H7NO2/c9-6-1-2-7-5(3-6)4-8(10)11-7/h1-3H,4,9H2

83528-03-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-amino-3H-1-benzofuran-2-one

1.2 Other means of identification

Product number -
Other names 3-aminocoumaranone

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:83528-03-4 SDS

83528-03-4Upstream product

83528-03-4Downstream Products

83528-03-4Relevant articles and documents

Intramolecular Cyclization of Arylnitrenium Ions. Formation of Carbon-Carbon Bonds and of Lactones

Abramovitch, Rudolph A.,Cooper, Melanie,Iyer, Suresh,Jeyaraman, Ramasubbu,Rodriguez, J. Augusto Rosario

, p. 4819 - 4820 (2007/10/02)

Arylnitrenium ions bearing a meta side chain heaving a suitable nucleophilic center are generated by the acid-catalyzed decomposition of the appropriate azide; they undergo intramolecular cyclization leading to new carbon-carbon bonds or to lactones in pr

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