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N(4)-acetylsulfamonomethoxine is a chemical compound derived from sulfamonomethoxine, an antimicrobial agent used in veterinary medicine. It is formed as a metabolite when sulfamonomethoxine is broken down in the body, specifically through the acetylation of the N(4) position. This metabolite possesses similar antimicrobial properties to its parent compound, targeting bacteria by inhibiting the synthesis of dihydrofolic acid, which is essential for bacterial growth. The presence of N(4)-acetylsulfamonomethoxine is significant in understanding the pharmacokinetics and efficacy of sulfamonomethoxine treatments, as it indicates the body's metabolic processing of the drug and can influence its overall effectiveness and safety profile.

4049-01-8

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4049-01-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4049-01-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,4 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4049-01:
(6*4)+(5*0)+(4*4)+(3*9)+(2*0)+(1*1)=68
68 % 10 = 8
So 4049-01-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H14N4O4S/c1-9(18)16-10-3-5-11(6-4-10)22(19,20)17-12-7-13(21-2)15-8-14-12/h3-8H,1-2H3,(H,16,18)(H,14,15,17)

4049-01-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-acetylamino-N-(6-methoxy-pyrimidin-4-yl)-benzenesulfonamide

1.2 Other means of identification

Product number -
Other names N-[4-(6-Methoxy-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamide

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:4049-01-8 SDS

4049-01-8Downstream Products

4049-01-8Relevant academic research and scientific papers

Preparation method for sulfanilamide-6-methoxy pyrimidine sodium

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Paragraph 0020-0022, (2017/01/23)

The present invention discloses a preparation method for a sulfanilamide-6-methoxy pyrimidine sodium-hydrate. The method specifically comprises the steps of: under the action of an organic base and pyridine, carrying out a reaction on 4-acetamido benzene sulfonyl chloride and 4-amino-6-methoxy pyrimidine to generate 4-acetamido benzene sulfanilamide-6-methoxy pyrimidine; then salifying with sodium hydroxide; and after decoloration treatment by activated carbon, cooling, crystallizing, filtrating and drying the product to obtain the sulfanilamide-6 a methoxy pyrimidine sodium hydrate. In the preparation method, a one-pot method is used for preparing sulfanilamide-6-methoxy pyrimidine sodium. Compared with the prior art at home, the synthetic steps are greatly simplified; furthermore, in the method provided by the invention, 4-MP and SCL are used as raw materials, occurrence of side reactions in a process of synthesizing sulfanilamide-6-methoxy pyrimidine sodium is avoided, thus effectively improving the yield of the product.

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