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N-(2-Pyridinyl)-N'-ethylthiourea is an organic compound with the chemical formula C8H11N3S. It is a derivative of thiourea, featuring a pyridine ring and an ethyl group attached to the nitrogen atoms. N-(2-Pyridinyl)-N'-ethylthiourea is known for its potential applications in chemical research and as a building block for the synthesis of various pharmaceuticals and agrochemicals. It is characterized by its ability to form coordination complexes with metal ions, which can be useful in the development of new materials with specific properties. The compound is typically synthesized through a reaction involving 2-pyridinecarboxylic acid and ethyl isothiocyanate, and it is important to handle it with care due to its potential toxicity and reactivity.

2741-10-8

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2741-10-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2741-10-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,4 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2741-10:
(6*2)+(5*7)+(4*4)+(3*1)+(2*1)+(1*0)=68
68 % 10 = 8
So 2741-10-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H11N3S/c1-2-9-8(12)11-7-5-3-4-6-10-7/h3-6H,2H2,1H3,(H2,9,10,11,12)

2741-10-8SDS

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 1-ethyl-3-pyridin-2-ylthiourea

1.2 Other means of identification

Product number -
Other names Thiourea,N-ethyl-N'-2-pyridinyl

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:2741-10-8 SDS

2741-10-8Downstream Products

2741-10-8Relevant academic research and scientific papers

Base Promoted Transformation on Thiadiazolopyridinium Chlorides

Martinez, Ana,Castro, Ana,Fayet

, p. 337 - 340 (1997)

1,2,4-Thiadiazolo[2,3-a]pyridinium chlorides undergo a very facile base promoted transformation to give bispyridilimino-1,2,4-thiadiazolidines. The unequivocal structural assignment of these last compounds was achieved by spectroscopic 1H, 13C and 15N two dimensional methods.

Synthesis and antimalarial efficacy of aza-fused rhodacyanines in vitro and in the P. berghei mouse model

Takasu, Kiyosei,Pudhom, Khanitha,Kaiser, Marcel,Brun, Reto,Ihara, Masataka

, p. 4795 - 4798 (2007/10/03)

Several aza-fused rhodacyanines were synthesized and assessed for their in vitro and in vivo antimalarial activities against Plasmodium falciparum K1 and P. berghei. All synthetic compounds showed strong selective antimalarial in vitro activity. Class II azarhodacyanines, 3, consisting of four heterocyclic units, were found to display good parasitemia suppression and low acute toxicity in vivo. Among them, 3c appeared to be the most effective at a dose of 20-25 mg kg-1 day-1 (ip).

New synthetic route to 1,2,4-thiadiazolines and 1,3- thiazolines via thiadiazolopyridinium salts

Martinez, Ana,Castro, Ana,Fonseca, Isabel,Ripoll, Martin Martinez-,Cano, Felix H.,Albert, Armando

, p. 2657 - 2666 (2007/10/03)

A new efficient synthesis of 1,2,4-thiadiazolidines and 1,3- thiazolidines bearing 2-pyridylimino substituents using thiadiazolopyridinium chlorides as intermediates is described. The mechanism probably involves a base promoted nucleophilic addition of thiadiazolopyridinium salts to nitriles and ketones.

Thiadiazolopyridinium Salts: Intermediates for Heterocyclic Synthesis

Castro, Ana,Martinez, Ana

, p. 1737 - 1740 (2007/10/02)

The high reactivity of thiadiazolopyridinium salts against electrophiles is described.This fact provides a new and efficient synthetic route to several heterocycles such as thiazolines, thiadiazolines and thiadiazolin-3-ones carrying pyridyl

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