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6028-97-3

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6028-97-3 Usage

Appearance

Yellow to brown solid

Odor

Strong

State

Solid

Usage

Commonly used as a reagent in organic synthesis

Potential applications

Medicinal chemistry

Biological activities

Anti-cancer and anti-inflammatory properties

Safety precautions

Harmful if ingested, inhaled, or absorbed through the skin

Potential hazards

May cause irritation to the eyes, skin, and respiratory system

Check Digit Verification of cas no

The CAS Registry Mumber 6028-97-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,2 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6028-97:
(6*6)+(5*0)+(4*2)+(3*8)+(2*9)+(1*7)=93
93 % 10 = 3
So 6028-97-3 is a valid CAS Registry Number.

6028-97-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-nitrophenyl)-1-thiophen-2-ylprop-2-en-1-one

1.2 Other means of identification

Product number -
Other names 1-(2-THIENYL)-3-(4-NITROPHENYL)-2-PROPEN-1-ONE

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:6028-97-3 SDS

6028-97-3Relevant articles and documents

ALLOSTERIC INHIBITORS OF ATYPICAL PROTEIN KINASES C

-

Paragraph 0090; 0108; 0139, (2015/06/08)

The invention provides specific small molecule compounds that allosterically regulate the activity of atypical protein kinase C, their use as a medicament, and their use in the treatment and prevention of allergic, inflammatory and autoimmune disorders, cancer, hyperproliferation, sepsis, viral and protozoan infections, dementing diseases, metabolic, sclerotic and osteoporotic disorders.

The effects of pendant vs. fused thiophene attachment upon the luminescence lifetimes and electrochemistry of tris(2,2′-bipyridine)ruthenium(II) complexes

Nurkkala, Lasse J.,Steen, Robert O.,Friberg, Henrik K. J.,Haeggstroem, Johanna A.,Bernhardt, Paul V.,Riley, Mark J.,Dunne, Simon J.

experimental part, p. 4101 - 4110 (2009/02/07)

The electrochemical and photophysical properties for a range of tris(2,2′-bipyridine)ruthenium(II) complexes in which a thiophene substituent is attached to one of the bipyridine ligands by either a pendant or a fused mode have been determined. The fused mode of attachment eliminates torsional movement between the thiophene unit and the chelating bipyridine, thereby offering optimal overlap between the ?-systems of the chelating unit and the attached thiophene unit. The electrochemical properties of these complexes were found to be similar; however, the luminescence lifetimes and intensities (in CH3CN at room temperature) were found to be correlated to the mode of attachment. The longest luminescence lifetime was observed for the complex [Ru(bpy)2{4-(thiophen-2-yl)-2,2′-bipyridine}] 2+ (3000 ns), as compared to the prototypic [Ru(bpy) 3]2+ (1745 ns). This complex also had the highest quantum yield (0.045). In the four isomeric complexes, where the thiophene ring was fused to the b or c face of the pyridine ring, the lifetimes fell in the interval 275-1510 ns, and the quantum yield ranged between 0.0047 and 0.014. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

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