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(2R,3S,5R)-5-(5-fluoro-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-(hydroxymethyl)tetrahydrofuran-3-yl benzoate is a complex organic compound with a molecular formula of C16H15FN2O6. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by its specific stereochemistry: the 2nd carbon (C2) is in the R configuration, the 3rd carbon (C3) is in the S configuration, and the 5th carbon (C5) is in the R configuration. (2R,3S,5R)-5-(5-fluoro-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-(hydroxymethyl)tetrahydrofuran-3-yl benzoate features a 5-fluoro-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl group, which is a derivative of pyrimidine with a fluorine atom and a dihydro structure. It also contains a 2-(hydroxymethyl)tetrahydrofuran-3-yl moiety, indicating the presence of a hydroxymethyl group attached to a tetrahydrofuran ring. The benzoate group suggests that it is an ester derived from benzoic acid. This chemical structure is likely to be found in pharmaceuticals or as an intermediate in the synthesis of biologically active compounds, given the presence of a fluorinated pyrimidine ring, which is a common structural motif in many drugs.

1995-83-1

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1995-83-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1995-83-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,9 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1995-83:
(6*1)+(5*9)+(4*9)+(3*5)+(2*8)+(1*3)=121
121 % 10 = 1
So 1995-83-1 is a valid CAS Registry Number.

1995-83-1Downstream Products

1995-83-1Relevant academic research and scientific papers

Studies directed toward the asialoglycoprotein receptor mediated delivery of 5-fluoro-2′-deoxyuridine for hepatocellular carcinoma

Rico, Lorena,?stergaard, Michael E.,Bell, Melanie,Seth, Punit P.,Hanessian, Stephen

, p. 2652 - 2654 (2018)

The anticancer nucleoside 5-fluoro 2′-deoxyuridine-5′-phosphate (5-FdU-P) was attached via an amide chain linker to a triantennary GalNAc cluster as a means to deliver the drug to hepatic cells that recognize the amino sugar units.

New 3′-O-aromatic acyl-5-fluoro-2′-deoxyuridine derivatives as potential anticancer agents

Szymańska-Michalak, Agnieszka,Wawrzyniak, Dariusz,Framski, Grzegorz,Kujda, Marta,Zgo?a, Paulina,Stawinski, Jacek,Barciszewski, Jan,Boryski, Jerzy,Kraszewski, Adam

, p. 41 - 52 (2016)

New aromatic and aliphatic 3′-O-acyl-5-fluoro-2′-deoxyuridine derivatives were synthesized and evaluated as candidates for prodrugs against various cancer cell lines. As the most promising candidate for antimalignant therapeutics was found a dual-acting a

Regioselective acylation of nucleosides and their analogs catalyzed by Pseudomonas cepacia lipase: enzyme substrate recognition

Li, Ning,Zong, Min-Hua,Ma, Ding

supporting information; experimental part, p. 1063 - 1068 (2009/04/11)

The substrate recognition of Pseudomonas cepacia lipase in the acylation of nucleosides was investigated by means of rational substrate engineering for the first time. P. cepacia lipase displayed excellent 3′-regioselectivities (96 to >99%) in the lauroyl

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