3-N-benzoyl-3',5'-di-O-benzoyl-5-(3-fluoropropyn-1-yl)-2'-deoxyuridine

Base Information

Chemical Name:3-N-benzoyl-3',5'-di-O-benzoyl-5-(3-fluoropropyn-1-yl)-2'-deoxyuridine
CAS No.:1037176-07-0
Molecular Formula:C₃₃H₂₅FN₂O₈
Molecular Weight:596.569
Hs Code.:

Synonyms:3-N-benzoyl-3',5'-di-O-benzoyl-5-(3-fluoropropyn-1-yl)-2'-deoxyuridine

Suppliers and Price of 3-N-benzoyl-3',5'-di-O-benzoyl-5-(3-fluoropropyn-1-yl)-2'-deoxyuridine

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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 3-N-benzoyl-3',5'-di-O-benzoyl-5-(3-fluoropropyn-1-yl)-2'-deoxyuridine

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Technology Process of 3-N-benzoyl-3',5'-di-O-benzoyl-5-(3-fluoropropyn-1-yl)-2'-deoxyuridine

There total 1 articles about 3-N-benzoyl-3',5'-di-O-benzoyl-5-(3-fluoropropyn-1-yl)-2'-deoxyuridine 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: 35.0%

: 1037176-06-9
3-N-benzoyl-3',5'-di-O-benzoyl-5-(3-hydroxypropyn-1-yl)-2'-deoxyuridine

: 1037176-07-0
3-N-benzoyl-3',5'-di-O-benzoyl-5-(3-fluoropropyn-1-yl)-2'-deoxyuridine

Guidance literature:: With 4,4'-diaminostilbene-2,2'-disulfonic acid; In dichloromethane; at -10 ℃; for 5h;
DOI:10.1021/jo800444y

Reference yield:

: 1037176-07-0
3-N-benzoyl-3',5'-di-O-benzoyl-5-(3-fluoropropyn-1-yl)-2'-deoxyuridine

: 1037176-19-4
3-N-benzoyl-3',5'-di-O-benzoyl-5-propyl-2'-deoxyuridine

: 1037176-10-5
3-N-benzoyl-3',5'-di-O-benzoyl-5-(3-fluoropropyl)-2'-deoxyuridine

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethyl acetate; at 20 ℃; for 5h; under 2068.65 Torr; Title compound not separated from byproducts.;
DOI:10.1021/jo800444y