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Ethyl 2-[(4-chlorobenzoyl)amino]-1-benzothiophene-3-carboxylate is a complex organic chemical compound with the molecular formula C18H14ClNO3S. It is a derivative of benzothiophene, a heterocyclic compound consisting of a benzene ring fused to a thiophene ring. The molecule features a 4-chlorobenzoyl group attached to the amino group, which in turn is connected to the benzothiophene core. ethyl 2-[(4-chlorobenzoyl)amino]-1-benzothiophene-3-carboxylate is characterized by its potential applications in the synthesis of pharmaceuticals and other organic compounds, as well as its unique chemical properties.

5525-28-0

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5525-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5525-28-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,2 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5525-28:
(6*5)+(5*5)+(4*2)+(3*5)+(2*2)+(1*8)=90
90 % 10 = 0
So 5525-28-0 is a valid CAS Registry Number.

5525-28-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-[(4-chlorobenzoyl)amino]-1-benzothiophene-3-carboxylate

1.2 Other means of identification

Product number -
Other names CCG-9846

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:5525-28-0 SDS

5525-28-0Relevant academic research and scientific papers

Anthraquinone intercalators as carrier molecules for second-generation platinum anticancer drugs

Gibson,Binyamin,Haj,Ringel,Ramu,Katzhendler

, p. 823 - 831 (2007/10/03)

A series of complexes PtAm2L [where Am2 = (NH3)2, ethylenediamine(en), 1,2-diaminocyclohexane (DACH) or (NH3)(c-C6H11NH2) and where L is a bidentate 1,1-dicarboxylate ligand tethered to 1- aminoanthraquinone by various spacers] was prepared and screened in vitro against P388 leukemia cells. The free ligands displayed moderate activity and the corresponding platinum complexes were tenfold more active. The nature of the linker chain does not seem to affect the potency of the complexes. The potency depends on the nature of the inert amine ligand [NH3 > DACH > en]. The low aqueous solubility of these complexes prevented any in vivo studies and the preparation of water soluble analogs is currently under way.

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