5'-O-dimethoxytrityl-2'-O-tetrahydropyranyl-N⁶-benzoyl-8-bromoadenosine

Base Information

Chemical Name:5'-O-dimethoxytrityl-2'-O-tetrahydropyranyl-N⁶-benzoyl-8-bromoadenosine
CAS No.:183320-32-3
Molecular Formula:C₄₃H₄₂BrN₅O₈
Molecular Weight:836.739
Hs Code.:

5'-O-dimethoxytrityl-2'-O-tetrahydropyranyl-N<sup>6</sup>-benzoyl-8-bromoadenosine

Synonyms:5'-O-dimethoxytrityl-2'-O-tetrahydropyranyl-N⁶-benzoyl-8-bromoadenosine

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 5'-O-dimethoxytrityl-2'-O-tetrahydropyranyl-N⁶-benzoyl-8-bromoadenosine

Chemical Property:

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Technology Process of 5'-O-dimethoxytrityl-2'-O-tetrahydropyranyl-N⁶-benzoyl-8-bromoadenosine

There total 8 articles about 5'-O-dimethoxytrityl-2'-O-tetrahydropyranyl-N⁶-benzoyl-8-bromoadenosine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 93.0%

: 40615-36-9
4,4'-dimethoxytrityl chloride

: 183320-27-6
2'-O-tetrahydropyranyl-N⁶-benzoyl-8-bromoadenosine

: 183320-32-3
5'-O-dimethoxytrityl-2'-O-tetrahydropyranyl-N⁶-benzoyl-8-bromoadenosine

Guidance literature:

Reference yield:

: 2946-39-6
8-bromoadenosine

: 183320-32-3
5'-O-dimethoxytrityl-2'-O-tetrahydropyranyl-N⁶-benzoyl-8-bromoadenosine

Guidance literature:: Multi-step reaction with 5 steps

3: H⁺

4: (C₂H₅)4NBr, KF

With potassium fluoride; tetraethylammonium bromide; hydrogen cation;

Reference yield:

: 165190-34-1
8-bromo-9-(3,5-O-tetraisopropyldisiloxane-1,3-diyl-β-D-ribofuranosyl)adenine

: 183320-32-3
5'-O-dimethoxytrityl-2'-O-tetrahydropyranyl-N⁶-benzoyl-8-bromoadenosine

Guidance literature:: Multi-step reaction with 4 steps

2: H⁺

3: (C₂H₅)4NBr, KF

With potassium fluoride; tetraethylammonium bromide; hydrogen cation;