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methyl (E)-3-oxo-2-((phenylamino)methylene)butanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87151-27-7

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87151-27-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87151-27-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,1,5 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 87151-27:
(7*8)+(6*7)+(5*1)+(4*5)+(3*1)+(2*2)+(1*7)=137
137 % 10 = 7
So 87151-27-7 is a valid CAS Registry Number.

87151-27-7Downstream Products

87151-27-7Relevant academic research and scientific papers

(E)-Methyl 2-anilinomethyl-ene-3-oxo-butanoate: X-ray and density functional theory studies

Langer, Vratislav,Scholtzova, Eva,Milata, Viktor,Solcan, Tomas

, p. o552-o554 (2007)

Mol-ecules of the title compound, C12H13NO3, are not planar and are stabilized by electrostatic inter-actions, as the dipole moment of the mol-ecule is 3.76 D. They are also stabilized by intra-molecular hydrogen bonds of N...O and C...O types, and by a complicated network of weak inter-molecular hydrogen bonds of the C...O type. This paper also reports the theoretical investigation of the hydrogen bonding and electronic structure of the title compound using natural bond orbital (NBO) analysis. International Union of Crystallography 2007.

An Efficient and Highly Diastereoselective Synthesis of GSK1265744, a Potent HIV Integrase Inhibitor

Wang, Huan,Kowalski, Matthew D.,Lakdawala, Ami S.,Vogt, Frederick G.,Wu, Lianming

supporting information, p. 564 - 567 (2015/03/04)

A novel synthesis of GSK1265744, a potent HIV integrase inhibitor, is described. The synthesis is highlighted by an efficient construction of the densely functionalized pyridinone core as well as a highly diastereoselective formation of the acyl oxazolidine moiety. The latter exploits the target molecules ability to chelate to Mg2+, a key feature in the integrase inhibitors mechanism of action.

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