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21278-85-3

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21278-85-3 Usage

Heterocyclic compound

Yes, it contains both nitrogen and sulfur atoms in its ring structure.

Ethyl ester derivative

Yes, it is derived from 2-(4-pyridinyl)-4-thiazolecarboxylic acid by attaching an ethoxy group to the carboxyl group.

Potential pharmaceutical applications

Yes, it has been studied for its potential as an antimicrobial and antifungal agent.

Potential as a precursor for the synthesis of other biologically active compounds

Yes, it can be used as a building block in the synthesis of other organic molecules.

Potential use as a ligand in coordination chemistry

Yes, it has been investigated for its ability to bind to metal ions.

Versatile compound

Yes, it has potential applications in medicinal chemistry, pharmaceuticals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 21278-85-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,7 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 21278-85:
(7*2)+(6*1)+(5*2)+(4*7)+(3*8)+(2*8)+(1*5)=103
103 % 10 = 3
So 21278-85-3 is a valid CAS Registry Number.

21278-85-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-pyridin-4-yl-1,3-thiazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names HMS557I01

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:21278-85-3 SDS

21278-85-3Relevant articles and documents

Discovery of Novel Aryl Carboxamide Derivatives as Hypoxia-Inducible Factor 1α Signaling Inhibitors with Potent Activities of Anticancer Metastasis

Liu, Mingming,Liang, Yuru,Zhu, Zhongzhen,Wang, Jin,Cheng, Xingxing,Cheng, Jiayi,Xu, Binpeng,Li, Rong,Liu, Xinhua,Wang, Yang

supporting information, p. 9299 - 9314 (2019/10/16)

In order to discover novel hypoxia-inducible factor 1 (HIF-1) inhibitors for the cancer metastasis treatment, 68 new aryl carboxamide compounds were synthesized and evaluated for their inhibitory effect by dual luciferase-reporter assay. Based on five rounds of investigation on structure-activity relationships step by step, compound 30m was discovered as the most active inhibitor (IC50 = 0.32 μM) with no obvious cytotoxicity (CC50 > 50 μM). It effectively attenuated hypoxia-induced HIF-1α protein accumulation and reduced transcription of vascular epidermal growth factor in a dose-dependent manner, which was further demonstrated by its inhibitory potency on capillary-like tube formation, angiogenesis of zebrafish as well as cellular migration and invasion. Importantly, compound 30m exhibited antimetastatic potency in breast cancer lung metastasis in the mice model, indicating its promising therapeutic potential for prevention and treatment of tumor metastasis. These results definitely merit attention for further rational design of more efficient HIF-1 inhibitors in the future.

HIV PROTEASE INHIBITING COMPOUNDS

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Page/Page column 156, (2010/02/12)

A compound of the formula (I) is disclosed as an HIV protease inhibitor. Methods and compositions for inhibiting an HIV infection are also disclosed.

2-oxo-1,3,4-trihydroquinazolinyl derivatives and methods of use

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Page 27, (2010/02/05)

Selected compounds are effective for treatment of diseases, such as cell proliferation or apoptosis mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable derivatives thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving stroke, cancer and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.

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