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Propanimidic acid, ethyl ester, also known as ethyl acetoacetate, is a chemical compound with the formula C6H10O3. It is a colorless liquid that is soluble in water and has a fruity odor. This ester is formed by the reaction of ethyl alcohol (ethanol) and acetoacetic acid, and it is widely used in the synthesis of various pharmaceuticals, dyes, and other organic compounds. Ethyl acetoacetate is an important intermediate in the preparation of barbiturates, a class of sedative and hypnotic drugs. It is also used in the production of certain pesticides and as a solvent in the paint and varnish industry. Due to its reactivity, ethyl acetoacetate can undergo various chemical transformations, making it a versatile building block in organic chemistry.

1070-17-3

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1070-17-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1070-17-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1070-17:
(6*1)+(5*0)+(4*7)+(3*0)+(2*1)+(1*7)=43
43 % 10 = 3
So 1070-17-3 is a valid CAS Registry Number.

1070-17-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl propanimidate

1.2 Other means of identification

Product number -
Other names ethyl propanimidoate

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:1070-17-3 SDS

1070-17-3Relevant academic research and scientific papers

Pop-the-Cork strategy in synthetic utilization of imines: Stabilization by complexation and activation via liberation of the ligated species

Bokach, Nadezhda A.,Kukushkin, Vadim Yu.,Haukka, Matti,Frausto da Silva, Joao J. R.,Pombeiro, Armando J. L.

, p. 3602 - 3608 (2003)

Treatment of trans-[PtCl4(RCN)2] (R = Me, Et) with ethanol allowed the isolation of trans-[PtCl4{E-NH=C(R)OEt}2]. The latter were reduced selectively, by the ylide Ph3P=CHCO2Me, to trans-[PtCl2{E-NH=C(R)OEt}2]. The complexed imino esters NH=C(R)OEt were liberated from the platinum(II) complexes by reaction with 2 equiv of 1,2-bis (diphenylphosphino)ethane (dppe) in chloroform; the cationic complex [Pt(dppe)2]Cl2 precipitates almost quantitatively from the reaction mixture and can be easily separated by filtration to give a solution of NH=C(R)OEt with a known concentration of the imino ester. The imino esters efficiently couple with the coordinated nitriles in trans-[PtCl4(EtCN)2] to give, as the dominant product, [PtCl4{NH=C(Et)N=C(R)OEt}2] containing a previously unknown linkage, i.e., ligated N-(1-imino-propyl)-alkylimidic acid ethyl esters. In addition to [PtCl4{NH=C(Et)N= C(Et)OEt}2], another compound was generated as the minor product, i.e., [PtCl4(EtCN){NH=(Et)N=C(Et)OEt}], which was reduced to [PtCl2(EtCN){NH=C(Et)N=C(Et)OEt}], and this complex was characterized by X-ray singlecrystal diffraction. The platinum(IV) complexes [PtCl4{NH=C(Et)N=C(R)OEt}2] are unstable toward hydrolysis and give EtOH and the acylamidine complexes trans-[PtCl4{Z-NH=C(Et)NHC(R)O}2], where the coordination to the Pt center results in the predominant stabilization of the imino tautomer NH=C(Et)NHC(R)=O over the other form, i.e., NH2C(Et)=NC(R)=O, which is the major one for free acylamidines. The structures of trans-[PtCl4{Z-NH=C(Et)NHC(R)=O}2] (R = Me, Et) were determined by X-ray studies. The complexes [PtCl4{NH=C(Et)N=C(R)OEt}2] were reduced to the appropriate platinum(II) compounds [PtCl2{NH=C(Et)N=C(R)OEt}2], which, similarly to the appropriate Pt(IV) compounds, rapidly hydrolyze to yield the acylamidine complexes [PtCl2{NH=C(Et)NHC(R)=O}2] and EtOH. The latter acylamidine compounds were also prepared by an alternative route upon reduction of the corresponding platinum(IV) complexes. Besides the first observation of the platinum(IV)-mediated nitrile-imine ester integration, this work demonstrates that the application of metal complexes gives new opportunities for the generation of a great variety of imines (sometimes unreachable in pure organic chemistry) in metal-mediated conversions of organonitriles, the storage of imino species in the complexed form, and their synthetic utilization after liberation.

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