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2-[(E)-Benzyloxyimino]-propionic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

178753-91-8

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178753-91-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 178753-91-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,7,5 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 178753-91:
(8*1)+(7*7)+(6*8)+(5*7)+(4*5)+(3*3)+(2*9)+(1*1)=188
188 % 10 = 8
So 178753-91-8 is a valid CAS Registry Number.

178753-91-8Relevant academic research and scientific papers

Syntheses of 2,3-dioxoalkylphosphonates and other novel β-ketophosphonates as well as of a phosphinopyruvamide (= (alkyloxyphosphinyl)pyruvamide)

Neidlein, Richard,Feistauer, Helmut

, p. 895 - 912 (1996)

The new 3-(diethoxyphosphoryl)-2-oxopropanoates 5 and 6 and -propanamides 1-4 with various amino substituents at C(3) were prepared (Scheme 2). These compounds exist, depending on N-substitution, as pure (E)-enols (in the case of 1 and 5) or as a mixture of three tautomeric forms (in the case of 1-4 and 6). The configuration could be unambiguously assigned from the 1H-, 13C-, and 31P-NMR spectra. Phosphinopyruvamide ( = (alkyloxyphosphinyl)pyruvamide) 9 was prepared in a similar manner in spite of the instability of phosphinate-derived carbanions. Some 3-(ethoxyimino)-2-oxobutylphosphonates, 11-13 (Scheme 5), and various 3,3-dimethoxy-2-oxoalkylphosphonates, 19-23 and 26-33 (Scheme 6), were available from the reaction of lithioalkylphosphonates with 2-(ethoxyimino)propanoates and 2,2-dimethoxyalkanoates, respectively. The 3,3-dimethoxybutylphosphonates 20, and 26-30 were cleaved to give 2,3-dioxobutylphosphonates 34-39 (Scheme 6). This method provides easy access to a new class of potentially pharmaceutically useful compounds.

1- And 2-Azetines via Visible Light-Mediated [2 + 2]-Cycloadditions of Alkynes and Oximes

Wearing, Emily R.,Blackmun, Dominique E.,Becker, Marc R.,Schindler, Corinna S.

supporting information, p. 16235 - 16242 (2021/10/20)

Azetines, four-membered unsaturated nitrogen-containing heterocycles, hold great potential for drug design and development but remain underexplored due to challenges associated with their synthesis. We report an efficient, visible light-mediated approach

N-(Aroyl)-N-(arylmethyloxy)-α-alanines: Selective inhibitors of aldose reductase

Nencetti, Susanna,La Motta, Concettina,Rossello, Armando,Sartini, Stefania,Nuti, Elisa,Ciccone, Lidia,Orlandini, Elisabetta

, p. 3068 - 3076 (2017/05/25)

Aldose reductase (ALR2), a NADPH-dependent reductase, is the first and rate-limiting enzyme of the polyol pathway of glucose metabolism and is implicated in the pathogenesis of secondary diabetic complications. In the last decades, this enzyme has been ta

Synthesis and antimicrobial properties of cephalosporin derivatives substituted on the C(7) nitrogen with arylmethyloxyimino or arylmethyloxyamino alkanoyl groups

Gentili, Daniela,Macchia, Marco,Menchini, Elisabetta,Nencetti, Susanna,Orlandini, Elisabetta,Rossello, Armando,Broccali, Giampietro,Limonta, Donatella

, p. 224 - 231 (2007/10/03)

Some 7-aminocephalosporanic acid (7-ACA) derivatives substituted on the C(7) nitrogen with 2-(arylmethyloxyimino)propionyl (3a-f), 2-(arylmethyloxyamino)propionyl (4a-d) and (arylmethyloxyamino)acetyl (2a-d) moieties were synthesized by reaction of the ap

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