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ethyl 2-(O-benzylhydroxylamino)-butanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73198-49-9

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73198-49-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73198-49-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,9 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73198-49:
(7*7)+(6*3)+(5*1)+(4*9)+(3*8)+(2*4)+(1*9)=149
149 % 10 = 9
So 73198-49-9 is a valid CAS Registry Number.

73198-49-9Relevant academic research and scientific papers

Multicomponent radical processes: Synthesis of substituted piperidinones

Godineau, Edouard,Landais, Yannick

, p. 12662 - 12663 (2007)

Three and four-component radical and radical-organometallic processes have been developed that provide a simple access to 2,3-disubstituted piperidinones. Reasonable yield and high stereoselectivities were achieved in a number of cases with three C-C bond

Intermolecular addition of alkyl radicals to imines in the absence and in the presence of a Lewis acid

Halland,Jorgensen

, p. 1290 - 1295 (2001)

The metal-catalyzed, and metal-catalyzed enantioselective, intermolecular additions of alkyl radicals to imines have been investigated. The reaction proceeds well for imines having both activating and deactivating nitrogen substituents, and can be controlled and accelerated to a high extent by the use of Lewis acids. For imines having different carbon substituents, it has been observed that those derived from glyoxylate react much faster than those derived from 3-oxopropionate or benzaldehyde. The intermolecular radical addition can be carried out for different types of imines with alkyl and alkoxyalkyl radicals and it is demonstrated that it is possible to perform the radical addition in a catalytic enantioselective fashion with moderate yield and enantioselectivity. On the basis of the experimental results and theoretical calculations the mechanism for the radical addition to imines is discussed.

Photoinduced Formation of β-Oxy-α,α-disubstituted-α-amino Acid Derivatives from Ketoximes

Torrente, Susana,Alonso, Ricardo

, p. 1985 - 1987 (2007/10/03)

(matrix presented) The first intermolecular radical addition onto ketoxime ethers is described. β-Oxygenated quaternary α-amino acid derivatives II were obtained upon irradiation of α-alkoxycarbonyl ketoxime ethers I in the presence of suitable α-alkoxy carbon radical precursors and a sensitizer.

α-Functionalized Amino Acid Derivatives. A Synthetic Approach of Possible Biogenetic Importance

Herscheid, Jacobus D. M.,Nivard, Rutger J. F.,Tijhuis, Marian W.,Scholten, Henk P. H.,Ottenheijm, Harry C. J.

, p. 1880 - 1885 (2007/10/02)

A new and efficient approach of general applicability to the synthesis of α-functionalized α-amino acid derivatives 3 is described.It is based upon the proposal that the biosynthesis of such compounds might occur via oxidation of an N-acylated amino acid

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