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2-PYRIDIN-2-YL-THIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

161772-80-1

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161772-80-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161772-80-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,7,7 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 161772-80:
(8*1)+(7*6)+(6*1)+(5*7)+(4*7)+(3*2)+(2*8)+(1*0)=141
141 % 10 = 1
So 161772-80-1 is a valid CAS Registry Number.

161772-80-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 2-(2'-pyridyl)-4-carbethoxythiazole

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:161772-80-1 SDS

161772-80-1Relevant academic research and scientific papers

I2/TBHP-Mediated tandem cyclization and oxidation reaction: Facile access to 2-substituted thiazoles and benzothiazoles

Liu, Li,Tan, Chen,Fan, Rong,Wang, Zihan,Du, Hongguang,Xu, Kun,Tan, Jiajing

supporting information, p. 252 - 256 (2019/01/10)

The efficient synthesis of 2-substituted thiazoles and benzothiazoles has been accomplished employing readily available cysteine esters and 2-aminobenzenethiols as N and S sources. The reaction proceeds under an I2/TBHP system and involves a on

Selective synthesis of 2-substituted 4-carboxy oxazoles, thiazoles and thiazolidines from serine or cysteine amino acids

Di Credico, Barbara,Reginato, Gianna,Gonsalvi, Luca,Peruzzini, Maurizio,Rossin, Andrea

experimental part, p. 267 - 274 (2011/02/26)

The synthesis of new 4-carboxy oxazoles, thiazoles and thiazolidines by condensation of serine or cysteine with aldehydes or acids is described. Due to the optimization of a mild and selective procedure, which takes advantage of the positive effect of mic

Design and synthesis of thiazole and thiazolidine metallo-supramolecular networks

Di Credico, Barbara,Gonsalvi, Luca,Peruzzini, Maurizio,Reginato, Gianna,Rossin, Andrea

scheme or table, p. 1312 - 1315 (2011/09/15)

A mild and selective procedure for the synthesis of 4-carboxy thiazoles and thiazolidines starting from naturally occurring cysteine by condensation with aldehydes is described. The optimized procedure, taking advantage of the positive effect of microwave

4-Alkoxycarbonyl-2-(2-pyridyl)thiazoles and their complexes with CuII and CoII. Molecular and crystal structure of copper 4-ethoxycarbonyl-2-(2-pyridyl) thiazole dichloride

Majouga,Beloglazkina,Frolov,Moiseeva,Zyk

experimental part, p. 844 - 850 (2010/08/08)

The first synthesis of ethyl 2-(2-pyridyl)thiazole-4-carboxylate (2) and bis[2-(2-pyridylthi-azol-4-ylcarbonyloxy)ethyl] disulfide (4) is described. The complexation of compounds 2 and 4 with CuII, CoII, and NiII chlorides and perchlorates has been studied. Electrochemical behavior of the ligands and complexes obtained has been investigated by cyclic voltammetry and using rotating disk electrode, which allowed us to confirm the possibility for the ligand 4 and its complexes to be adsorbed on the surface of a gold electrode.

HIV PROTEASE INHIBITING COMPOUNDS

-

Page/Page column 105, (2010/02/12)

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

HIV protease inhibiting compounds

-

Page/Page column 97, (2010/02/12)

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

HIV protease inhibiting compounds

-

Page/Page column 130, (2010/02/12)

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

HIV PROTEASE INHIBITING COMPOUNDS

-

Page/Page column 158, (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.

Synthesis of 2-substituted-4-carbethoxythiazoles

Kim, Hong-Seok,Kwon, Il-Cheon,Kim, Oh-Hwoan

, p. 937 - 940 (2007/10/03)

In the presence of boron trifluoride etherate, aryl and alkylthioamides react with ethyl diazopyruvate to give high yields of corresponding thiazoles.

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