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(5E)-5-{[1-(3-chlorophenyl)-2,5-dimethyl-1H-pyrrol-3-yl]methylidene}-2-thioxo-1,3-thiazolidin-4-one is a complex organic compound with a molecular formula of C18H14ClNOS2. It features a 1,3-thiazolidin-4-one core structure, which is a five-membered heterocyclic ring containing sulfur and nitrogen atoms. The compound has a 5-(E)-alkene group, indicating the presence of a double bond between the 5th and 6th carbon atoms. Additionally, it contains a 3-chlorophenyl group attached to a 2,5-dimethyl-1H-pyrrol-3-yl moiety, which is a substituted pyrrole ring. This molecule is characterized by its unique structure and potential applications in various chemical and pharmaceutical fields.

6053-97-0

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6053-97-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6053-97-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,5 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6053-97:
(6*6)+(5*0)+(4*5)+(3*3)+(2*9)+(1*7)=90
90 % 10 = 0
So 6053-97-0 is a valid CAS Registry Number.

6053-97-0SDS

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,N-diethyl-Ethenamine

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6053-97-0 SDS

6053-97-0Relevant academic research and scientific papers

Photochemical and photophysical regularities of reduction of acetone with triethylamine

Markaryan

, p. 1012 - 1016 (2007/10/03)

The data on chemically induced dynamic polarization of nuclei (CIDPN) obtained in this work and the available data on chemically induced dynamic polarization of electrons (CIDPE) are used to examine photochemical and photophysiscal processes involved in the reduction of acetone by triethylamine (TEA). The time-resolved CIDPN method is used to study the efficiency of TEA as a chemical quencher and the effect of laser radiation intensity (308 nm) on polarization processes and the composition of the reaction products. The relative reactivities of the acetone T1 and S1 states depend on the TEA concentration and the laser irradiation intensity: at [TEA] 1.5 mol/l, singlet acetone molecules are also effectively quenched. At high irradiation intensities, the α-cleavage of triplet acetone also occurs via a two-photon process. The mechanism developed involves reverse proton transfer, disproportionation, and recombination with the participation of radical pairs and agrees with the CIDPN effects observed in experiment.

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