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Butanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl](phenylmethoxy)amino]-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

122148-93-0

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122148-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122148-93-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,1,4 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 122148-93:
(8*1)+(7*2)+(6*2)+(5*1)+(4*4)+(3*8)+(2*9)+(1*3)=100
100 % 10 = 0
So 122148-93-0 is a valid CAS Registry Number.

122148-93-0Downstream Products

122148-93-0Relevant academic research and scientific papers

Thermodynamic Stability and Speciation of Ga(III) and Zr(IV) Complexes with High-Denticity Hydroxamate Chelators

Albanese, Valentina,Baldi, Andrea,Fritsky, Igor O.,Guerrini, Remo,Gumienna-Kontecka, Elzbieta,Illuminati, Davide,Mular, Andrzej,Ostrowska, Ma?gorzata,Pacifico, Salvatore,Piasta, Karolina,Remelli, Maurizio,Toporivska, Yuliya

, p. 13332 - 13347 (2021)

Increasing attention has been recently devoted to 89Zr(IV) and 68Ga(III) radionuclides, due to their favorable decay characteristics for positron emission tomography (PET). In the present paper, a deep investigation is presented on Ga(III) and Zr(IV) comp

Rational Design, Development, and Stability Assessment of a Macrocyclic Four-Hydroxamate-Bearing Bifunctional Chelating Agent for 89Zr

Seibold, Uwe,W?ngler, Bj?rn,W?ngler, Carmen

, p. 1555 - 1571 (2017/09/26)

Zirconium-89 is a positron-emitting radionuclide of high interest for medical imaging applications with positron emission tomography (PET). For the introduction of this radiometal into biologically active targeting vectors, the chelating agent desferrioxa

Octadentate Zirconium(IV)-Loaded Macrocycles with Varied Stoichiometry Assembled From Hydroxamic Acid Monomers using Metal-Templated Synthesis

Tieu, William,Lifa, Tulip,Katsifis, Andrew,Codd, Rachel

supporting information, p. 3719 - 3728 (2017/03/24)

The reaction between Zr(IV) and the forward endo-hydroxamic acid monomer 4-[(5-aminopentyl)(hydroxy)amino]-4-oxobutanoic acid (for-PBH) in a 1:4 stoichiometry in the presence of diphenylphosphoryl azide and triethylamine gave the octadentate Zr(IV)-loaded tetrameric hydroxamic acid macrocycle for-[Zr(DFOT1)] ([M + H]+ calc 887.3, obs 887.2). In this metal-templated synthesis (MTS) approach, the coordination preferences of Zr(IV) directed the preorganization of four oxygen-rich bidentate for-PBH ligands about the metal ion prior to ring closure under peptide coupling conditions. The replacement of for-PBH with 5-[(5-aminopentyl) (hydroxy)amino]-5-oxopentanoic acid (for-PPH), which contained an additional methylene group in the dicarboxylic acid region of the monomer, gave the analogous Zr(IV)-loaded macrocycle for-[Zr(PPDFOT1)] ([M + H]+ calc 943.4, obs 943.1). A second, well-resolved peak in the liquid chromatogram from the for-PPH MTS system also characterized as a species with [M + H]+ 943.3, and was identified as the octadentate complex between Zr(IV) and two dimeric tetradentate hydroxamic acid macrocycles for-[Zr(PPDFOT1D)2]. Treatment of for-[Zr(PPDFOT1)] or for-[Zr(PPDFOT1D)2] with EDTA at pH 4.0 gave the respective hydroxamic acid macrocycles as free ligands: octadentate PPDFOT1 or two equivalents of tetradentate PPDFOT1D (homobisucaberin, HBC). At pH values closer to physiological, EDTA treatment of for-[Zr(DFOT1)], for-[Zr(PPDFOT1)], or Zr(IV) complexes with related linear tri- or tetrameric hydroxamic acid ligands showed the macrocycles were more resistant to the release of Zr(IV), which has implications for the design of ligands optimized for the use of Zr(IV)-89 in positron emission tomography (PET) imaging of cancer.

Evaluation of hadacidin analogues

Tibrewal, Nidhi,Elliott, Gregory I.

supporting information; experimental part, p. 517 - 519 (2011/02/25)

Several derivatives of hadacidin have been developed and evaluated for activity against adenylosuccinate synthetase.

ALKYLATION OF N-BENZYLOXYUREAS AND CARBAMATES

Sulsky, Richard,Demers, James P.

, p. 31 - 34 (2007/10/02)

N-benzyloxyureas and orthogonically protected N-hydroxycarbamates can be alkylated in high yields and subsequently deprotected to provide N-alkyl hydroxyureas and hydroxylamines.

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