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benzyl 4-((tert-butoxycarbonyl)amino)-1-methyl-1H-imidazole-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

128293-65-2

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128293-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128293-65-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,2,9 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 128293-65:
(8*1)+(7*2)+(6*8)+(5*2)+(4*9)+(3*3)+(2*6)+(1*5)=142
142 % 10 = 2
So 128293-65-2 is a valid CAS Registry Number.

128293-65-2Relevant academic research and scientific papers

Highly efficient synthesis of DNA-binding polyamides using a convergent fragment-based approach

Fallows, Andrew J.,Singh, Ishwar,Dondi, Ruggero,Cullis, Paul M.,Burley, Glenn A.

, p. 4654 - 4657 (2014)

Two advances in the synthesis of hairpin pyrrole-imidazole polyamides (PAs) are described. First, the application of a convergent synthetic strategy is shown, involving the Boc-based solid phase synthesis of a C-terminal fragment and the solution phase synthesis of the N-terminal fragment. Second a new hybrid resin is developed that allows for the preparation of hairpin PAs lacking a C-terminal β-alanine tail. Both methods are compatible with a range of coupling reagents and provide a facile, modular route to prepare PA libraries in high yield and crude purity.

4-Methyltrityl-Protected Pyrrole and Imidazole Building Blocks for Solid Phase Synthesis of DNA-Binding Polyamides

Heinrich, Benedikt,Vázquez, Olalla

, p. 533 - 536 (2020/01/31)

DNA-binding polyamides are synthetic oligomers of pyrrole/imidazole units with high specificity and affinity for double-stranded DNA. To increase their synthetic diversity, we report a mild methodology based on 4-methyltrityl (Mtt) solid phase peptide synthesis (SPPS), whose building blocks are more accessible than the standard Fmoc and Boc SPPS ones. We demonstrate the robustness of the approach by preparing and studying a hairpin with all precursors. Importantly, our strategy is orthogonal and compatible with sensitive molecules and could be readily automated.

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