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N-(2-hydroxyethyl)-3-(5-nitrofuran-2-yl)prop-2-enamide is a complex organic compound with the molecular formula C10H10N2O5. It is a derivative of furan, a heterocyclic aromatic organic compound, and features a nitro group (-NO2) attached to the furan ring. The molecule also contains a prop-2-enamide group, which is a three-carbon chain with a double bond and an amide group. Additionally, it has a 2-hydroxyethyl group attached to the nitrogen atom, which contributes to its hydrophilic properties. N-(2-hydroxyethyl)-3-(5-nitrofuran-2-yl)prop-2-enamide is known for its potential antimicrobial and antifungal properties, making it a subject of interest in pharmaceutical research. However, it is important to note that the safety and efficacy of N-(2-hydroxyethyl)-3-(5-nitrofuran-2-yl)prop-2-enamide in medical applications would require thorough testing and regulatory approval.

6755-17-5

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6755-17-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6755-17-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,5 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6755-17:
(6*6)+(5*7)+(4*5)+(3*5)+(2*1)+(1*7)=115
115 % 10 = 5
So 6755-17-5 is a valid CAS Registry Number.

6755-17-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-N-(2-hydroxyethyl)-3-(5-nitrofuran-2-yl)prop-2-enamide

1.2 Other means of identification

Product number -
Other names 3t-(5-Nitro-[2]furyl)-acrylsaeure-(2-hydroxy-aethylamid)

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:6755-17-5 SDS

6755-17-5Downstream Products

6755-17-5Relevant academic research and scientific papers

5-Nitrofuranes and 5-nitrothiophenes with anti-trypanosoma cruzi activity and ability to accumulate squalene

Gerpe, Alejandra,álvarez, Guzmán,Benítez, Diego,Boiani, Lucía,Quiroga, Martín,Hernández, Paola,Sortino, Maximiliano,Zacchino, Susana,González, Mercedes,Cerecetto, Hugo

experimental part, p. 7500 - 7509 (2011/02/24)

Chagas disease represents a serious public health problem in South America. The first line of treatment is Nifurtimox and Benznidazole which generate toxic effects in treated patients. We have recently shown that a number of 5-nitrofuranes possess activity against Trypanosoma cruzi through oxidative stress and inhibition of parasite ergosterol biosynthesis, specifically at the level of squalene epoxidase. Here, we identify new 5-nitrofuranes and the thia-analogues with excellent effects on the viability of T. cruzi and adequate parasite/mammal selectivity indexes. Analysis of the free sterols from parasite incubated, during 120 h, with the compounds showed that some of them accumulated squalene suggesting the squalene epoxidase activity inhibition of the parasite. Nifurtimox was able to accumulate squalene only at lower incubation times. Due to this fact some derivatives were also tested as antifungal agents. Quantitative structure-activity relationship studies were also performed showing relevant features for further new derivatives design. Taken together, the results obtained in the present work point to a more general effect of 5-nitrofuranes and 5-nitrothiophenes in trypanosomatids, opening potential therapeutic possibilities of them for these infectious diseases.

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