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104892-41-3

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104892-41-3 Usage

General Description

ETHYL 2-[(ANILINOCARBOTHIOYL)AMINO]ACETATE is a chemical compound with the molecular formula C12H15N3O2S. It is a derivative of aniline, a common building block in organic chemistry. The compound contains a carbonyl group, an amino group, and a thioester group, making it versatile for use in various chemical reactions and synthetic processes. It is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and dyes. Additionally, it has been studied for its potential anti-inflammatory and anti-cancer properties. The compound is a white to off-white solid and is typically handled and stored under strict laboratory conditions due to its potential reactivity and toxicity.

Check Digit Verification of cas no

The CAS Registry Mumber 104892-41-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,8,9 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 104892-41:
(8*1)+(7*0)+(6*4)+(5*8)+(4*9)+(3*2)+(2*4)+(1*1)=123
123 % 10 = 3
So 104892-41-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N2O2S/c1-2-15-10(14)8-12-11(16)13-9-6-4-3-5-7-9/h3-7H,2,8H2,1H3,(H2,12,13,16)

104892-41-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(phenylcarbamothioylamino)acetate

1.2 Other means of identification

Product number -
Other names ethylanilinocarbothioylaminoacetate

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:104892-41-3 SDS

104892-41-3Relevant articles and documents

An Improved Protocol for Synthesis of 3-Substituted 5-Arylidene-2-thiohydantoins: Two-step Procedure Alternative to Classical Methods

Kuznetsova, Olga Yu,Antipin, Roman L.,Udina, Anna V.,Krasnovskaya, Olga O.,Beloglazkina, Elena K.,Terenin, Vladimir I.,Koteliansky, Victor E.,Zyk, Nikolay V.,Majouga, Alexander G.

, p. 1570 - 1577 (2016/09/24)

A novel method for the direct synthesis of 5-arylidene-2-thiohydantoins from thioureas and aromatic aldehydes in the presence of base in ethanol was developed. Application of this efficient method allowed preparing thiohydantoins, which are difficult to s

Synthesis of 3-ω-amino-2-thiohydantoins

Ryczek, Jozef

, p. 665 - 670 (2007/10/03)

In the reaction of ethyl isothiocyanatoacetate with diamines, followed by cyclization of the intermediate product, 3-monosubstituted thiohydantoins have been obtained. It was found that the reaction course depends on the purity of the isothiocyanate used and also, in the case of dialkylaminoamines, the self-cyclization occurs. Besides the dialkylamino derivatives of 3-monosubstituted 2-thiohydantoins also new monoalkylamino, amino and heterocyclic derivatives were synthesized. The aryldiazonium derivative of 3-monosubstituted 2-thiohydantoin yielded both respective phenol derivative after hydrolysis and the product of coupling with 2-naphthol.

BASE CATALYZED CYCLIZATION OF SUBSTITUTED ESTERS OF HYDANTOIC AND THIOHYDANTOIC ACID

Kavalek, Jaromir,Machacek, Vladimir,Svobodova, Gabriela,Sterba, Vojeslav

, p. 375 - 390 (2007/10/02)

Base catalyzed cyclization rates have been measured of 22 derivatives of hydantoic and thiohydantoic acid esters in water and methanol.The cyclization of methyl and ethyl esters of hydantoic and 5-methylhydantoic acids is accompanied by hydrolysis of the ester group, whereas with the other derivatives the hydrolysis does not take place.Hydrolysis of the cyclization products (hydantoin and thiohydantoin derivatives) is not significant under the kinetic conditions.The cyclization of methyl ester of 5-phenylhydantoic acid in methanol is reversible; the equilibrium mixture contains 30percent of the starting ester.In all the cases the cyclization is subject to specific base catalysis; exceptions are esters of 5-phenylthiohydantoic and 5-phenyl-2-methylthiohydantoic acids whose cyclizations are subject to general base catalysis.Substituents always accelerate the cyclization.The 3-substituents have the greatest effects, the cyclization rate being considerably increased with bulk of the substituents; similarly large effect of 5-phenyl group consists mainly in its polar effects on the pre-equilibrium.The cyclizations are slower in methanol at the same concentration of the lyate ion: the greatest difference (up to 3 orders of magnitude) is observed with the 5-phenyl derivatives.

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