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Home  > Adenosine 5'-(trihydrogen diphosphate), 2'-(dihydrogen phosphate), P'→5'-ester with 1,4-dihydro-1-β-D-ribofuranosyl-3-pyridinecarboxamide, compd. with cyclohexanamine (1:4)

AE11448

100929-71-3 | Adenosine 5'-(trihydrogen diphosphate), 2'-(dihydrogen phosphate), P'→5'-ester with 1,4-dihydro-1-β-D-ribofuranosyl-3-pyridinecarboxamide, compd. with cyclohexanamine (1:4)

Packsize Purity Availability Price Discounted Price    Quantity
5mg 95% in stock $43.00 $30.00 -   +
10mg 95% in stock $80.00 $56.00 -   +
25mg 95% in stock $125.00 $88.00 -   +
50mg 95% in stock $212.00 $148.00 -   +
100mg 95% in stock $369.00 $259.00 -   +
250mg 95% in stock $560.00 $392.00 -   +
1g 95% in stock $1,432.00 $1,002.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AE11448
Chemical Name: Adenosine 5'-(trihydrogen diphosphate), 2'-(dihydrogen phosphate), P'→5'-ester with 1,4-dihydro-1-β-D-ribofuranosyl-3-pyridinecarboxamide, compd. with cyclohexanamine (1:4)
CAS Number: 100929-71-3
Molecular Formula: C45H82N11O17P3
Molecular Weight: 1142.1173630000012
MDL Number: MFCD00079504
SMILES: O[C@@H]1[C@H](O)[C@H](O[C@H]1N1C=CCC(=C1)C(=O)N)COP(=O)(OP(=O)(OC[C@H]1O[C@H]([C@@H]([C@@H]1O)OP(=O)(O)O)n1cnc2c1ncnc2N)O)O.NC1CCCCC1.NC1CCCCC1.NC1CCCCC1.NC1CCCCC1

 

Upstream Synthesis Route
  • Adenosine 5'-(trihydrogen diphosphate), 2'-(dihydrogen phosphate), P'→5'-ester with 1,4-dihydro-1-β-D-ribofuranosyl-3-pyridinecarboxamide, compd. with cyclohexanamine (1:4) is a versatile compound used in chemical synthesis for its ability to act as a precursor in the formation of specialized nucleotides. This compound plays a crucial role in the assembly of nucleic acids, which are essential molecules that carry genetic information within living organisms.In chemical synthesis, this complex compound serves as a key building block for the creation of nucleotide analogs and modified nucleic acids. By incorporating this compound into synthetic processes, chemists can tailor the properties of nucleotides to suit specific research or therapeutic applications. Additionally, the presence of cyclohexanamine in the compound further enhances its reactivity and potential applications in diverse chemical transformations.Overall, the strategic utilization of Adenosine 5'-(trihydrogen diphosphate), 2'-(dihydrogen phosphate), P'→5'-ester with 1,4-dihydro-1-β-D-ribofuranosyl-3-pyridinecarboxamide, compd. with cyclohexanamine (1:4) in chemical synthesis enables researchers to expand their toolkit for molecular manipulation and design, opening up new possibilities for drug discovery, materials science, and biochemical research.
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