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2,3-Dihydro-1-benzofuran-5-sulfonamide, a benzofuran derivative with the molecular formula C8H9NO3S, is an organic compound characterized by a benzene ring fused to a furan ring. The presence of a sulfonamide group, which consists of a sulfur atom double-bonded to an oxygen and bonded to a nitrogen atom, with the nitrogen atom attached to the benzofuran ring, endows this compound with unique structural features. Its potential biological activities and applications in medicinal chemistry or pharmaceutical research are of interest, although further studies are required to fully understand its properties and uses.

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  • 112894-47-0 Structure
  • Basic information

    1. Product Name: 2,3-DIHYDRO-1-BENZOFURAN-5-SULFONAMIDE
    2. Synonyms: 2,3-DIHYDRO-1-BENZOFURAN-5-SULFONAMIDE;2,3-Dihydrobenzo[b]furan-5-sulphonamide;5-Benzofuransulfonamide,2,3-dihydro-(9CI)
    3. CAS NO:112894-47-0
    4. Molecular Formula: C8H9NO3S
    5. Molecular Weight: 199.23
    6. EINECS: N/A
    7. Product Categories: SULFONAMIDE
    8. Mol File: 112894-47-0.mol
  • Chemical Properties

    1. Melting Point: 164-166°C
    2. Boiling Point: 402.3°Cat760mmHg
    3. Flash Point: 197.1°C
    4. Appearance: /
    5. Density: 1.438g/cm3
    6. Vapor Pressure: 1.1E-06mmHg at 25°C
    7. Refractive Index: 1.611
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 10.34±0.20(Predicted)
    11. CAS DataBase Reference: 2,3-DIHYDRO-1-BENZOFURAN-5-SULFONAMIDE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2,3-DIHYDRO-1-BENZOFURAN-5-SULFONAMIDE(112894-47-0)
    13. EPA Substance Registry System: 2,3-DIHYDRO-1-BENZOFURAN-5-SULFONAMIDE(112894-47-0)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 112894-47-0(Hazardous Substances Data)

112894-47-0 Usage

Uses

Used in Pharmaceutical Research:
2,3-Dihydro-1-benzofuran-5-sulfonamide is used as a chemical entity in pharmaceutical research for its potential to contribute to the development of new drugs. Its unique structure may offer novel binding properties and interactions with biological targets, which could be harnessed to create therapeutic agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2,3-dihydro-1-benzofuran-5-sulfonamide is utilized as a compound with the potential to be modified and optimized for specific medicinal applications. Its chemical properties and structural features can be further explored and manipulated to enhance its pharmacological profile.
Note: Since the provided materials do not specify particular applications or industries for 2,3-Dihydro-1-benzofuran-5-sulfonamide, the uses listed are general and based on the potential of the compound's structure and properties in the context of pharmaceutical research and medicinal chemistry. Further information would be needed to detail specific applications or industries.

Check Digit Verification of cas no

The CAS Registry Mumber 112894-47-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,8,9 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 112894-47:
(8*1)+(7*1)+(6*2)+(5*8)+(4*9)+(3*4)+(2*4)+(1*7)=130
130 % 10 = 0
So 112894-47-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO3S/c9-13(10,11)7-1-2-8-6(5-7)3-4-12-8/h1-2,5H,3-4H2,(H2,9,10,11)

112894-47-0SDS

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 2,3-Dihydro-1-benzofuran-5-sulfonamide

1.2 Other means of identification

Product number -
Other names 2,3-DICHLORO-3'-PYRROLIDINOMETHYL BENZOPHENONE

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:112894-47-0 SDS

112894-47-0Relevant articles and documents

Diarylsulfonylureas for use in treating secretory diarrhea

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, (2008/06/13)

This invention provides methods of treating secretory diarrhea or cystic fibrosis in a mammal which comprises administering to a mammal in need thereof an effective amount of diarylsulfonylurea. This invention also describes specific diarylsulfonylureas f

Antitumor compositions and methods of treatment

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, (2008/06/13)

This invention provides certain sulfonamidoquinoxaline derivatives and methods for using them in the treatment of susceptible neoplasms in mammals. Also provided are certain novel pharmaceutical formulations employing these sulfonamidoquinoxaline derivatives, in combination with a carrier, diluent or excipient.

Synthesis of bicyclic aromatic sulfonic acids sulfonyl chlorides and sulfonamides

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, (2008/06/13)

This invention provides a novel process for the synthesis of bicyclic aromatic sulfonic acids employing reacting a bicyclic aromatic compound with sulfur trioxide-N,N-dimethylformamide complex in the presence of a water miscible, non-reactive solvent. The resulting sulfonic acid may be converted into the corresponding sulfonyl halide by the reaction with a thionyl halide. This invention further provides a novel process for the synthesis of bicyclic aromatic sulfonamides employing the reaction conditions described supra followed by an ammonolysis or amination.

Antitumor compositions and methods

-

, (2008/06/13)

This invention provides the use of N-[[(3,4-dichlorophenyl)amino]carbonyl]-2,3-dihydrobenzofuran-5-sulfonamide, and pharmaceutically acceptable salts thereof, in the treatment of susceptible neoplasms in mammals. This invention further provides the novel aforementioned compound and its pharmaceutical formulations.

Antitumor compositions and methods of treatment

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, (2008/06/13)

This invention provides the use of certain tetra-substituted imidazolidin-2-one derivatives in the treatment of susceptible neoplasms in mammals. Also provided are certain novel tetra-substituted imidazolidin-2-one derivatives and pharmaceutical formulati

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