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The chemical compound "3-Adenylic acid, N-benzoyl-5-O-(bis(4-methoxyphenyl)phenylmethyl)-P-(4-chlorophenyl)-2-deoxyadenylyl-(3.5)-N-benzoyl-2-deoxy-,4-chlorophenyl 2-cyanoethyl ester" is a complex organic molecule with a long and specific name. It is a derivative of adenylic acid, which is a nucleotide that plays a crucial role in various biological processes, including energy transfer and signal transduction. This particular compound features a benzoyl group attached to the nitrogen atom, a bis(4-methoxyphenyl)phenylmethyl group at the 5' position, and a 4-chlorophenyl group at the phosphorus atom. The 2-deoxyadenylyl moiety is connected to the 3.5 position, and the molecule is further modified with a 2-cyanoethyl ester group. 3-Adenylic acid, N-benzoyl-5-O-(bis(4-methoxyphenyl)phenylmethyl)-P-(4-chlorophenyl)-2-deoxyadenylyl-(3.5)-N-benzoyl-2-deoxy-,4-chlorophenyl 2-cyanoethyl ester is likely to be of interest in the field of medicinal chemistry, potentially as a precursor or intermediate in the synthesis of therapeutic agents, due to its intricate structure and the presence of various functional groups that can interact with biological targets.

71459-59-1

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71459-59-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71459-59-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,4,5 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 71459-59:
(7*7)+(6*1)+(5*4)+(4*5)+(3*9)+(2*5)+(1*9)=141
141 % 10 = 1
So 71459-59-1 is a valid CAS Registry Number.

71459-59-1Downstream Products

71459-59-1Relevant academic research and scientific papers

Synthesis of Deoxyoligonucleotide Linker Fragments for Genetic Engineering Using Improved Preparative and Analytical Techniques

Seliger, Hartmut,Bach, Trung-Chinh,Siewert, Gerhard,Boidol, Werner,Toepert, Michael,et al.

, p. 835 - 853 (2007/10/02)

For studies on the expression of recombinant DNA, linker fragments have been prepared which serve to introduce specific points of cleavage on the DNA as well as the protein level.Such linkers were designed for cyanogen bromide as well as for collagenase cleavage of fused proteins.The preparation was done according to the triester synthesis scheme using improved and simpler routes to functionalized dinucleotide building blocks.Field desorption mass spectrometry was used as a routine tool for the identification and control of the purity of these units.

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