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N-(4-methylphenyl)-3-nitrobenzenesulfonamide is a chemical compound with the molecular formula C13H12N2O4S. It is a derivative of benzenesulfonamide, featuring a nitro group at the 3-position and a 4-methylphenyl group attached to the nitrogen atom. Benzenesulfonamide, N-(4-methylphenyl)-3-nitro- is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, particularly as an intermediate in the production of various active ingredients. Its chemical structure endows it with specific properties that can be exploited in chemical reactions, making it a valuable component in the development of new compounds with desired therapeutic or pesticidal effects.

4284-46-2

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4284-46-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4284-46-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,8 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4284-46:
(6*4)+(5*2)+(4*8)+(3*4)+(2*4)+(1*6)=92
92 % 10 = 2
So 4284-46-2 is a valid CAS Registry Number.

4284-46-2SDS

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 3-nitro-benzenesulfonic acid p-toluidide

1.2 Other means of identification

Product number -
Other names 3-Nitro-benzolsulfonsaeure-p-toluidid

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:4284-46-2 SDS

4284-46-2Relevant academic research and scientific papers

BENZENESULFONAMIDE DERIVATIVES AS TRAP1 MODULATORS AND USES THEREOF

-

Paragraph 00297; 00303-00305, (2021/09/26)

The present disclosure provides compounds of Formula (I): and pharmaceutically acceptable salts, solvates, hydrates, polymorphs, co-crystals, tautomers, stereoisomers, isotopically labeled compounds, and prodrugs thereof. The provided compounds may be tumor necrosis factor ("TNF") receptor associated protein 1 ("TRAP1") modulators (e.g., TRAP1 activators). The provided compounds may also rescue the activity in PTEN-induced kinase 1 ("PINK1") loss of function contexts. The provided compounds may also improve mitochondrial health, function, quality, quantity, and/or activity, and/or reduce the production of reactive oxygen species. The provided compounds may also refold or solubilize aggregated or misfolded proteins such as α-synuclein. The present disclosure also provides pharmaceutical compositions comprising the provided compounds; kits comprising the provided compounds or pharmaceutical compositions; and methods of using the provided compounds and pharmaceutical compositions (e.g., for treating a disease in a subject in need thereof).

Combined Effect of the Reactant Structure and Medium on Kinetics of Acylation of Arylamines with Arenesulfonyl Chlorides

Kustova,Kuritsyn

, p. 604 - 606 (2007/10/03)

A correlation equation was obtained for the logarithm of the rate constant of acylation of arylamines with arenesulfonyl chlorides in relation to the reactant structure and the nature of the medium. The reliability of this equation for calculation of the rate constants was confirmed by an additional kinetic study of the reactions of arylamines with arenesulfonyl chlorides in propanol, tert-butyl alcohol, and acetonitrile.

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