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Acetamide, N-[4-[[(3-methoxypyrazinyl)amino]sulfonyl]phenyl]-, also known as compound 1, is a complex organic chemical compound with the molecular formula C13H14N4O4S. It is characterized by a pyrazine ring, a methoxy group, and a sulfonyl group attached to a phenyl ring, which is further connected to an acetamide group. Acetamide, N-[4-[[(3-methoxypyrazinyl)amino]sulfonyl]phenyl]- is of interest in the field of medicinal chemistry, particularly in the development of potential therapeutic agents. Its structure and properties make it a candidate for further research in drug discovery, as it may exhibit specific biological activities or interactions with target proteins. The compound's exact role and application in pharmaceuticals or other industries would depend on its specific properties, which are not detailed in this summary.

655-78-7

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655-78-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 655-78-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,5 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 655-78:
(5*6)+(4*5)+(3*5)+(2*7)+(1*8)=87
87 % 10 = 7
So 655-78-7 is a valid CAS Registry Number.

655-78-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-acetylamino-N-(3-methoxy-pyrazin-2-yl)-benzenesulfonamide

1.2 Other means of identification

Product number -
Other names 2-(N'-Acetyl-p-aminobenzolsulfonamido)-3-methoxy-pyrazin

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:655-78-7 SDS

655-78-7Relevant academic research and scientific papers

Necrosulfonamide inhibits necroptosis by selectively targeting the mixed lineage kinase domain-like protein

Liao, Daohong,Sun, Liming,Liu, Weilong,He, Sudan,Wang, Xiaodong,Lei, Xiaoguang

supporting information, p. 333 - 337 (2014/03/21)

Through high-throughput screening of 200000 compounds and subsequent structure-activity relationship (SAR) studies we identified necrosulfonamide (NSA) as a potent small molecule inhibitor for necroptosis, induced by a combination of TNF-a, Smac mimetic, and z-VAD-fmk (T/S/Z). Applying a forward chemical genetic approach, we utilized an NSA based chemical probe to further reveal that NSA selectively targeted the Mixed Lineage Kinase Domain-like Protein (MLKL) to block the necrosome formation.

Sulfonamide molecular crystals: Structure, sublimation thermodynamic characteristics, molecular packing, hydrogen bonds networks

Perlovich, German L.,Ryzhakov, Alex M.,Tkachev, Valery V.,Hansen, Lars Kr.,Raevsky, Oleg A.

, p. 4002 - 4016 (2013/09/24)

The crystal structures of ten sulfonamides have been determined by X-ray diffraction. On the basis of our previous data, the obtained results and literature data crystal properties including molecular conformational states, packing architecture, and hydrogen bond networks were comparatively analyzed using graph set notations. Conformational flexibility of the bridge connecting two phenyl rings was studied. It was found out that the most frequently occurring graphs for compounds with a single hydrogen bond are infinite chains with four atoms included. The molecular packing architecture of the selected crystals may be conditionally divided into three different groups. The idea underlying such classification is the difference in structure and composition of molecular layers that can be singled out for most packings. The influence of various molecular fragments on crystal lattice energy was analyzed. A correlation between melting points and fragmental molecular interactions in the crystal lattices was obtained. The thermodynamic aspects of the sulfonamide sublimation were studied by determining the temperature dependence of vapor pressure using the transpiration method. A correlation between the Gibbs energy of the sublimation process and the melting points was found. Besides, a regression equation was derived to describe the correlation between the sublimation entropy terms and crystal density data calculated from X-ray diffraction results.

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