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N-[4-[[[(4-acetamidophenyl)sulfonylamino]carbamoylamino]sulfamoyl]phenyl]acetamide is a complex organic compound with the molecular formula C18H20N6O7S2. It is a derivative of acetamide, featuring a sulfonyl group, a carbamoyl group, and a sulfamoyl group attached to a phenyl ring. N-[4-[[[(4-acetamidophenyl)sulfonylamino]carbamoylamino]sulfamoyl]phenyl]acetamide is characterized by its unique structure, which includes a 4-acetamidophenyl group connected to a sulfonylamino moiety, which in turn is linked to a carbamoylamino group and a sulfamoyl group. The compound's structure contributes to its potential applications in various fields, such as pharmaceuticals or chemical research, due to its ability to form strong hydrogen bonds and its potential reactivity with other molecules.

5444-89-3

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5444-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5444-89-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5444-89:
(6*5)+(5*4)+(4*4)+(3*4)+(2*8)+(1*9)=103
103 % 10 = 3
So 5444-89-3 is a valid CAS Registry Number.

5444-89-3SDS

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 N-[4-[[[(4-acetamidophenyl)sulfonylamino]carbamoylamino]sulfamoyl]phenyl]acetamide

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

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More Details:5444-89-3 SDS

5444-89-3Downstream Products

5444-89-3Relevant academic research and scientific papers

A convenient procedure for the preparation of sulfonamidoureas using triphosgene

Safaei-Ghomi, Javad,Bamoniri, Abdolhamid,Abbaszadeh-Nooshabady, Aboalfazl

, p. 721 - 724 (2008/10/09)

An efficient method for the preparation of sulfonamidourea using triphosgene in organic solvents is reported. Sulfonylhydrazides and acetylsulfanilylhydrazide were transformed into the corresponding intermediates using triphosgene in 1,4-dioxane/water or tetrahydrofuran as solvents. These intermediates were converted in situ into symmetrical and unsymmetrical sulfonamidoureas in high yields and shorter periods of time related to previous methods.

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