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N-(3-methyl-4-sulfamoylphenyl)acetamide is a synthetic organic compound that belongs to the sulfonamide class. It has a molecular formula of C10H12N2O3S and features functional groups such as the sulfamoyl and acetamide groups. N-(3-methyl-4-sulfamoylphenyl)acetamide's primary application and properties may vary depending on the context of its use and the compounds it is combined with. Its sulfamoylphenyl structure suggests a potential relationship with antibacterial activity, as sulfonamides are recognized for their antibacterial properties in medicine. However, more comprehensive studies are needed to understand its specific uses, toxicity, and safety measures.

5433-02-3

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5433-02-3 Usage

Uses

Used in Pharmaceutical Industry:
N-(3-methyl-4-sulfamoylphenyl)acetamide is used as a potential antibacterial agent for its sulfonamide structure, which is known for its antibacterial properties in medicine.
Used in Chemical Research:
N-(3-methyl-4-sulfamoylphenyl)acetamide is used as a research compound for studying the properties and applications of sulfonamide-based compounds in various chemical and biological contexts.

Check Digit Verification of cas no

The CAS Registry Mumber 5433-02-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5433-02:
(6*5)+(5*4)+(4*3)+(3*3)+(2*0)+(1*2)=73
73 % 10 = 3
So 5433-02-3 is a valid CAS Registry Number.

5433-02-3SDS

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 2,2-bis(3-methylbut-2-enoxy)ethylbenzene

1.2 Other means of identification

Product number -
Other names 5(acetamido)-2-methyl-benzenesulfonamide

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:5433-02-3 SDS

5433-02-3Relevant academic research and scientific papers

1-PHENYLPYRROLE COMPOUNDS

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Page/Page column 41-42, (2010/04/28)

The present invention comprises a compound for the prevention and/or treatment of cardiovascular diseases, nephropathy, fibrosis, primary aldosteronism or edema. The compound is of the following general formula (I): wherein R1 represents a C1 -C3 alkyl group; R2 represents a hydroxy -C1 -C4 alkyl group and the like; R3 represents a halogeno group, a halogeno-C1 -C3 alkyl group and the like; R4 represents a hydrogen atom, a halogeno group and the like,- R5 represents a sulfamoyl group or a C1-C3 alkylsulf onyl group; R6 represents a hydrogen atom, a halogeno group and the like] or an N-oxide, atropisomer of the foregoing, or pharmaceutically acceptable salt of the foregoing.

ANTIPROLIFERATIVE 2-(SULFO-PHENYL)-AMINOTHIAZOLE DERIVATIVES

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Page 76-77, (2010/02/08)

Aminothiazole compounds substituted with sulfur-containing groups are represented by the Formula (I), and their pharmaceutically acceptable salts, prodrugs, active metabolites, and pharmaceutically acceptable salts of said metabolites are described. These agents modulate and/or inhibit the cell proliferation and activity of protein kinases and are useful as pharmaceuticals for treating malignancies and other disorders.

New processes for the synthesis of 2,6-dichloro-3- methylaniline-Ph-UL-14C and methyl 6-chloroanthranilate-Ph-UL-14C

McKendry,Stanga

, p. 1157 - 1164 (2007/10/02)

Two new processes were developed for the synthesis of 2,6-dichloro-3-methylaniline-Ph-UL-14C (1), a key intermediate in the synthesis of a DowElanco experimental product presently being considered for commercialization. Both processes afford product in much higher yields than that previously reported in the literature. One of the processes was subsequenly applied to the synthesis of methyl 6-chloroanthranilate-Ph-14C (12), used as an intermediate for a second potential product.

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