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phenylmethyl [(1S)-2-phenyl-1-[(2S)-tetrahydro-5-oxo-2-furanyl]ethyl]carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

143601-50-7

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143601-50-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143601-50-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,6,0 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 143601-50:
(8*1)+(7*4)+(6*3)+(5*6)+(4*0)+(3*1)+(2*5)+(1*0)=97
97 % 10 = 7
So 143601-50-7 is a valid CAS Registry Number.

143601-50-7Relevant academic research and scientific papers

SmI2-mediated couplings of α-amino acid derivatives. Formal synthesis of (-)-pumiliotoxin 251D and (±)-epiquinamide

Pinho, Vagner D.,Procter, David J.,Burtoloso, Antonio C. B.

supporting information, p. 2434 - 2437 (2013/06/27)

The coupling between cyclic and acyclic α-amino acid derivatives and methyl acrylate, mediated by samarium diiodide, is described. The method constitutes a powerful tool to construct indolizidine, quinolizidine, and piperidine systems in a straightforward two-step fashion. The formal synthesis of (-)-pumiliotoxin 251D and (±)-epiquinamide is achieved after two or three steps from these amino acid derivatives.

Formal total synthesis of the potent renin inhibitor aliskiren: Application of a SmI2-promoted acyl-like radical coupling

Lindsay, Karl B.,Skrydstrup, Troels

, p. 4766 - 4777 (2007/10/03)

A formal total synthesis of the potent renin inhibitor aliskiren is disclosed exploiting an alternative coupling strategy recently developed by this laboratory for the preparation of the hydroxyethylene isostere-based class of protease inhibitors. The thi

A stereodivergent synthesis of hydroxyethylene dipeptide isostere via highly diastereoselective epoxidation

Lee, Kyu Woong,Choi, Hyeong-Wook,Lee, Byung Han,Choi, Bo Seung,Chang, Jay Hyok,Kim, Young Keun,Lee, Jae Hoon,Heo, Taeho,Nam, Do Hyun,Shin, Hyunik

, p. 3136 - 3138 (2007/10/03)

Epoxidation of δ-amino-β,γ-unsaturated ester with trifluoroperacetic acid afforded its epoxide in a highly diastereoselective manner. Subsequent stereodivergent epoxide opening reactions provided synthetic routes towards both the threo and erythro hydroxy

A SIMPLE SYNTHETIC APPROACH TO Cbz-Phe-Ψ-(CH2)Gly-Pro-OMe AND RELATED PEPTIDE ISOSTERES

Hoffman, Robert V.,Kim, Hwa-Ok

, p. 3579 - 3582 (2007/10/02)

A new approach to ketomethylene and hydroxymethylene peptide isosteres has been developed which is simple, direct, and highly convergent.A key feature is construction of the central bond of a γ-keto ester by alkylation of a t-butyl β-keto ester with an α-bromo ester.

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