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555-25-9

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555-25-9 Usage

Description

4-(Acetylamino)-N-(2,6-dimethoxy-4-pyrimidinyl)benzenesulfonamide is a chemical compound with a complex structure, characterized by its benzene ring, sulfonyl group, and various substituents. It is a derivative of sulfonamide, a class of antimicrobial agents, and possesses potential pharmaceutical and industrial applications.

Uses

Used in Pharmaceutical Industry:
4-(Acetylamino)-N-(2,6-dimethoxy-4-pyrimidinyl)benzenesulfonamide is used as an active pharmaceutical ingredient for its antimicrobial properties. It is particularly effective against a range of bacterial infections due to its ability to inhibit bacterial growth and proliferation.
Used in Aquaculture:
In the aquaculture industry, 4-(Acetylamino)-N-(2,6-dimethoxy-4-pyrimidinyl)benzenesulfonamide is used as a preventive measure to control the spread of diseases in freshwater fish populations. It is often combined with other drugs, such as Ormetoprim, to enhance its efficacy and prevent the development of antibiotic-resistant strains.
Used in Chemical Synthesis:
4-(Acetylamino)-N-(2,6-dimethoxy-4-pyrimidinyl)benzenesulfonamide can also be utilized as a key intermediate in the synthesis of various other chemical compounds, including those with potential applications in the pharmaceutical, agrochemical, and materials science industries. Its unique structure and functional groups make it a valuable building block for the development of new molecules with specific properties and functions.
Used in Research and Development:
Due to its structural complexity and potential applications, 4-(Acetylamino)-N-(2,6-dimethoxy-4-pyrimidinyl)benzenesulfonamide is a valuable compound for research and development purposes. Scientists and researchers can use it to study its properties, investigate its interactions with biological systems, and explore its potential uses in various fields, including drug discovery, materials science, and environmental applications.

Check Digit Verification of cas no

The CAS Registry Mumber 555-25-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,5 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 555-25:
(5*5)+(4*5)+(3*5)+(2*2)+(1*5)=69
69 % 10 = 9
So 555-25-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H16N4O5S/c1-9(19)15-10-4-6-11(7-5-10)24(20,21)18-12-8-13(22-2)17-14(16-12)23-3/h4-8H,1-3H3,(H,15,19)(H,16,17,18)

555-25-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[4-[(2,6-dimethoxypyrimidin-4-yl)sulfamoyl]phenyl]acetamide

1.2 Other means of identification

Product number -
Other names 4-<N4-Acetyl-sulfanilamino>-2,6-dimethoxy-pyrimidin

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:555-25-9 SDS

555-25-9Downstream Products

555-25-9Relevant articles and documents

A sulfonamide - 2, 6 - dimethoxy pyrimidine preparation method (by machine translation)

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Paragraph 0023-0026; 0032-0034; 0038; 0039; 0043; 0044, (2017/12/05)

The invention relates to a sulfonamide - 2, 6 - dimethoxy pyrimidine of the preparation method, the 4 - amino - 2, 6 - dimethoxy pyrimidine and P-acetyl amino sulfonyl chloride in N, N - dimethyl formamide and the presence of triethylamine, in the 15 - 20 °C reaction under 10 - 14 hours, then post-processed to obtain 4 - P-acetyl amino sulfonamide - 2, 6 - dimethoxy pyrimidine; will be 4 - P-acetyl amino sulfonamide - 2, 6 - dimethoxy pyrimidine in methanol and the mass concentration is 15% -25% of sodium hydroxide solution in the presence of, in 85 - 90 °C reaction 5 - 7 hours, then post-processed to obtain the sulfonamide - 2, 6 - dimethoxy pyrimidine. The invention the synthetic route and the optimization of the process conditions and the like, so that the realization of the kg sulfonamide - 2, 6 - dimethoxy pyrimidine at the time of preparation, sulfonamide - 2, 6 - dimethoxy pyrimidine yield and purity of the still very high, is suitable for industrial production. (by machine translation)

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