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18529-17-4

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18529-17-4 Usage

General Description

ETHYL 3-(4-FLUOROANILINO)CROTONATE is an organic compound with the chemical formula C13H13NO3F. It is a derivative of crotonic acid and contains a fluorine-substituted aniline group. ETHYL 3-(4-FLUOROANILINO)CROTONATE is commonly used as a precursor in the synthesis of pharmaceuticals and agrochemicals. It has potential applications in the development of drugs for various therapeutic purposes, including anti-inflammatory and analgesic properties. Additionally, its unique chemical structure makes it valuable in the field of organic chemistry for the creation of new molecules with diverse biological activities. Overall, ETHYL 3-(4-FLUOROANILINO)CROTONATE is an important building block for the creation of various valuable compounds in the pharmaceutical and agrochemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 18529-17-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,5,2 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18529-17:
(7*1)+(6*8)+(5*5)+(4*2)+(3*9)+(2*1)+(1*7)=124
124 % 10 = 4
So 18529-17-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H14FNO2/c1-3-16-12(15)8-9(2)14-11-6-4-10(13)5-7-11/h4-8,14H,3H2,1-2H3/b9-8+

18529-17-4 Well-known Company Product Price

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  • Alfa Aesar

  • (A18251)  Ethyl 3-(4-fluoroanilino)crotonate, 97%   

  • 18529-17-4

  • 1g

  • 203.0CNY

  • Detail
  • Alfa Aesar

  • (A18251)  Ethyl 3-(4-fluoroanilino)crotonate, 97%   

  • 18529-17-4

  • 5g

  • 716.0CNY

  • Detail
  • Alfa Aesar

  • (A18251)  Ethyl 3-(4-fluoroanilino)crotonate, 97%   

  • 18529-17-4

  • 25g

  • 2859.0CNY

  • Detail

18529-17-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 3-(4-fluoroanilino)crotonate, 98%

1.2 Other means of identification

Product number -
Other names ethyl 3-(N-4-fluorophenyl)aminobut-2-enoate

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 -
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More Details:18529-17-4 SDS

18529-17-4Relevant articles and documents

Facile one-pot multicomponent synthesis of highly functionalized tetrahydropyridines using thiamine hydrochloride as an organocatalyst

Singh, Sandeep,Gupta, Annah,Kapoor, Kamal K.

, p. 1056 - 1063 (2020)

Thiamine hydrochloride (VitB1) has been found to be an efficient catalyst for the multicomponent synthesis of highly functionalized tetrahydropyridines from the reaction of β-ketoester, aromatic aldehydes and anilines. VitB1 is easily available, cheap, and eco benign.

Ecofriendly and facile Nano ZnO catalyzed solvent-free enamination of 1,3-dicarbonyls

Indulkar, Utkarsha U.,Kale, Sandip R.,Gawande, Manoj B.,Jayaram, Radha V.

supporting information; experimental part, p. 3857 - 3860 (2012/08/27)

Nano zinc oxide (Nano-ZnO) was explored as a reusable catalyst for the enamination of 1,3-dicarbonyls using diverse amines. To make the process environmentally viable, the reaction was carried out under solvent-free conditions and found to give good yield of desired products. The catalyst was characterized by various analytical techniques such as UV-spectroscopy, XRD, and TEM. The catalyst was found to be reusable up to four catalytic cycles without any appreciable loss in activity.

A facile, chemoselective and eco-friendly solid phase synthesis of enaminones catalyzed by L-Proline

Bhupathi, Raja S.,Devi, B.Rama,Dubey

experimental part, p. 5521 - 5524 (2012/07/13)

A facile and chemoselective method for the synthesis of enaminones by the reaction of aromatic primary amines with various β-ketoesters in the presence of L-proline as activator under solid phase is described. The reactions are promoted by the catalyst in short time (5-6 min) under ambient conditions, without any side products.

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