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NSC 178900, also known as a nitrated thiophene derivative, is a chemical compound with brown solid properties. It is primarily recognized for its applications as a parasiticide and as an intermediate in the synthesis of Nercrosulfonamide (N388600) analogue.
[Data of usage]:
Used in Pharmaceutical Industry:
NSC 178900 is used as an intermediate in the synthesis of Nercrosulfonamide (N388600) analogue for its role in the development of pharmaceutical compounds.
Used in Veterinary Medicine:
NSC 178900 is used as a parasiticide for the treatment and control of parasitic infections in animals, contributing to improved animal health and productivity.
Used in Chemical Synthesis:
NSC 178900, being a nitrated thiophene derivative, is used as a chemical intermediate in the synthesis of various other compounds, expanding its utility in the chemical industry.

17163-22-3

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17163-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17163-22-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,6 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17163-22:
(7*1)+(6*7)+(5*1)+(4*6)+(3*3)+(2*2)+(1*2)=93
93 % 10 = 3
So 17163-22-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H5NO4S/c9-7(10)4-2-5-1-3-6(13-5)8(11)12/h1-4H,(H,9,10)/b4-2+

17163-22-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-(5-nitrothiophen-2-yl)prop-2-enoic acid

1.2 Other means of identification

Product number -
Other names 5-Nitro-thienyl-(2)>-acrylsaeure

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:17163-22-3 SDS

17163-22-3Downstream Products

17163-22-3Relevant academic research and scientific papers

New fluorescent crosslinked aromatic polyamides containing thiopheneand furane in their backbone

Sánchez,Sobarzo,Gatica,Mac-Leod-carey

, p. 3040 - 3044 (2015)

New fluorescent crosslinked aromatic polyamides containing phenylen, thiophene and furane groups in the main chain were synthesized by self-condensation from 3-(5-aminothiophen-2-yl)propenoic acid, 3-(5-aminofuran-2-yl)propenoic acid and 3-(4-((5-aminothiophen-2-yl)methyleneamino)phenyl)propenoic acid using the phosphorylation method and triphenylphosphite as initiator. The amino compounds were obtained from 3-(5-nitrothiophen-2-yl)propenoic acid, 3-(5-nitrofuran-2-yl)propenoic acid and 3-(4-((5-nitrothiophen-2-yl)methyleneamino)phenyl)propenoic by selective reduction of each nitro group and was confirmed by 1H-NMR and FT-IR spectroscopy. Crosslinking of polyamides ocurr by mechanism between vinyl side groups reacts with the vinyl carbon of another chain, giving rise to interchain linear crosslinking. Depending on the structure the polymers have higher degree of crosslinking. Some vinyl groups react by thermal treatmentat 200 °C. Partially crosslinked polyamides with high emission fluorescence were obtained. Consequently amide bond formation, crosslinking and conjugation are the main factors that influence the fluorescence process. While polymers have several factors that affect the fluorescence, we believe that the most significant is the crosslinking of vinyl bonds. Subsequent thermal treatment of polyamides provoked crosslinking increase and fluorescence loss. The effect of the chemical structure was correlated with the thermal decomposition. Polyamides were characterized by UV-visible, FT-IR and 1H-NMR spectroscopy, inherent viscosity and thermogravimetric analysis (TGA). The synthesized polyamides exhibited potential for heat sensitive devices application since the fluorescence can be activated or quenched according to a heating process.

PROPENAMIDE THIOPHENE DERIVATIVES AS FLAVIVIRUS INHIBITORS AND THEIR USE

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Page/Page column 19; 20; 21, (2017/07/06)

The present invention deals with new flavivirus inhibitors, compositions comprising said inhibitors and methods for the treatment of disorders related to a viral infection, such as a disease due to a flavivirus infection, comprising administering said inhibitors.

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