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CAS

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52147-91-8

Ethenesulfonamide, 2-(4-nitrophenyl)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 52147-91-8 Structure

  • Basic information

    1. Product Name: Ethenesulfonamide, 2-(4-nitrophenyl)-, (E)-
    2. Synonyms:
    3. CAS NO:52147-91-8
    4. Molecular Formula: C8H8N2O4S
    5. Molecular Weight: 228.229
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 52147-91-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Ethenesulfonamide, 2-(4-nitrophenyl)-, (E)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethenesulfonamide, 2-(4-nitrophenyl)-, (E)-(52147-91-8)
    11. EPA Substance Registry System: Ethenesulfonamide, 2-(4-nitrophenyl)-, (E)-(52147-91-8)

  • 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: 52147-91-8(Hazardous Substances Data)

52147-91-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52147-91-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,1,4 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 52147-91:
(7*5)+(6*2)+(5*1)+(4*4)+(3*7)+(2*9)+(1*1)=108
108 % 10 = 8
So 52147-91-8 is a valid CAS Registry Number.

52147-91-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-nitrophenyl)ethenesulfonamide

1.2 Other means of identification

Product number -
Other names Ethenesulfonamide,2-(4-nitrophenyl)-,(E)

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:52147-91-8 SDS

52147-91-8Relevant articles and documents

Green approach for the synthesis of thiophenyl pyrazoles and isoxazoles by adopting 1,3-dipolar cycloaddition methodology and their antimicrobial activity

Sowmya,Lakshmi Teja,Padmaja,Kamala Prasad,Padmavathi

, p. 891 - 898 (2018)

A variety of N-((1,3-diphenyl-5-aryl-1H-pyrazol-4-yl)sulfonyl)thiophene-2-carboxamides (7) and N-((5-aryl-3-phenylisoxazol-4-yl)sulfonyl)thiophene-2-carboxamides (8) were prepared from (E)-N-(arylethenesulfonyl)thiophene-2-carboxamides (4) adopting 1,3-di

Arylation and alkenylation of activated alkyl halides using sulfonamides

Greaney, Michael F.,Johnson, Stuart,Kovács, Ervin

supporting information, p. 3222 - 3224 (2020/03/23)

A variety of quaternary aryl amino acid derivatives can be synthesised using tandem SN2/Smiles rearrangement chemistry involving aryl sulfonamides and α-chloro carbonyl compounds. The reaction harnesses a sulfur dioxide extrusion pathway to construct a C-N and C-Caryl bond under simple conditions with no requirement for organometallics or transition metal catalysts. The reaction is also successful for alkenyl sulfonamides, producing sterically congested quaternary alkene amino acid derivatives.

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