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4-[(2,4-Dichlorophenyl)sulfonyl]benzenamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 105456-57-3 Structure
  • Basic information

    1. Product Name: 4-[(2,4-Dichlorophenyl)sulfonyl]benzenamine
    2. Synonyms: 4-[(2,4-Dichlorophenyl)sulfonyl]aniline;4-[(2,4-Dichlorophenyl)sulfonyl]benzenamine
    3. CAS NO:105456-57-3
    4. Molecular Formula: C12H9Cl2NO2S
    5. Molecular Weight: 302.18
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 105456-57-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 494.0±45.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.481±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 0.53±0.10(Predicted)
    10. CAS DataBase Reference: 4-[(2,4-Dichlorophenyl)sulfonyl]benzenamine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-[(2,4-Dichlorophenyl)sulfonyl]benzenamine(105456-57-3)
    12. EPA Substance Registry System: 4-[(2,4-Dichlorophenyl)sulfonyl]benzenamine(105456-57-3)
  • 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: 105456-57-3(Hazardous Substances Data)

105456-57-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105456-57-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,4,5 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 105456-57:
(8*1)+(7*0)+(6*5)+(5*4)+(4*5)+(3*6)+(2*5)+(1*7)=113
113 % 10 = 3
So 105456-57-3 is a valid CAS Registry Number.

105456-57-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2,4-dichlorophenyl)sulfonylaniline

1.2 Other means of identification

Product number -
Other names -

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:105456-57-3 SDS

105456-57-3Downstream Products

105456-57-3Relevant articles and documents

SMALL MOLECULE ACTIVATORS OF NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE (NAMPT) AND USES THEREOF

-

, (2018/08/03)

Provided herein are small molecule activators of Nicotinamide Phosphoribosyltransferase (NAMPT), compositions comprising the compounds, and methods of using the compounds and compositions.

Quantitative Structure-Activity Analysis in Dihydropteroate Synthase Inhibition by Sulfones. Comparison with Sulfanilamides

Benedetti, Pier G. De,Iarossi, Dario,Menziani, Cristina,Caiolfa, Valeria,Frassineti, Chiara,Cennamo, Carlo

, p. 459 - 464 (2007/10/02)

A set of 25 4'-, eight 2',4'-, and five 2',4',6'-substituted 4-aminodiphenyl sulfones were tested for their inhibitory activity on dihydropteroate synthase of Escherichia coli.Linear regression analysis shows that enzymic inhibition indices correlate well with both quantum chemical and spectroscopic descriptors of the electronic structure of the common moiety 4-NH2-C6H4-SO2 of the sulfones (the above descriptors being expressed in relation to the electronic structure of the enzyme substrate, p-aminobenzoate).Therefore, the biological activity of the sulfones can be related to the electronic structural resemblance between these inhibitors and the substrate of the target enzyme.Since a similar result was previously obtained for a wide series of sulfanilamides in their different (amidic, imidic, and anionic) forms, it appears possible to consider the antibacterial sulfones and sulfanilamides as a congeneric chemical series.On the basis of the present results, the classical theory of antimetabolites would appear to take on a quantitative and sound rationale.

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