133510-52-8

Basic information

• Product Name: 3-Benzoyl-1-((2R,4S,5R)-5-hydroxymethyl-4-methylsulfanylmethoxy-tetrahydro-furan-2-yl)-5-methyl-1H-pyrimidine-2,4-dione
• CAS NO: 133510-52-8
• Molecular Weight: 406.459
• Mol File: 133510-52-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-Benzoyl-1-((2R,4S,5R)-5-hydroxymethyl-4-methylsulfanylmethoxy-tetrahydro-furan-2-yl)-5-methyl-1H-pyrimidine-2,4-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Benzoyl-1-((2R,4S,5R)-5-hydroxymethyl-4-methylsulfanylmethoxy-tetrahydro-furan-2-yl)-5-methyl-1H-pyrimidine-2,4-dione(133510-52-8)
• EPA Substance Registry System: 3-Benzoyl-1-((2R,4S,5R)-5-hydroxymethyl-4-methylsulfanylmethoxy-tetrahydro-furan-2-yl)-5-methyl-1H-pyrimidine-2,4-dione(133510-52-8)

Safety Data

• Hazardous Substances Data: 133510-52-8(Hazardous Substances Data)

Upstream product

• 40615-39-2 5'-O-(4-4'-dimethoxytrityl)thymidine 
• 98-88-4 benzoyl chloride 
• 130867-58-2 Methoxy-acetic acid (2R,3S,5R)-5-(3-benzoyl-5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-tetrahydro-furan-3-yl ester 
• 130867-60-6 5'-O-dimethoxytrityl-3'-O-(4-pentenyloxymethyl)-N³-benzoyl-thymidine 
• 130867-57-1 5’-O-dimethoxytrityl-3’-O-methoxyacetylthymidine 
• 102573-69-3 5'-O-(4-4'-dimethoxytrityl)-N³-benzoyl thymidine 
• 130867-59-3 5'-O-dimethoxytrityl-3'-O-methylthiomethyl-N³-benzoyl-thymidine 

Downstream Products

• 133510-53-9 5'-O-levulinoyl-3'-O-methylthiomethyl-N³-benzoyl-thymidine 
• 133510-59-5 C₆₁H₆₄N₆O₂₂ 

Relevant articles and documents

An efficient approach to the synthesis of thymidine derivatives containing phosphate-isosteric methylene acetal linkages

Iodonium ion promoted condensation of properly protected 3′-O-methylthiomethyl or 3′-O-(4-penten-1-oxymethyl)-thymidine with 3′-O-methoxyacetyl-thymidine, was explored. A judicious choice of the iodoinium source and protecting groups led to an efficient preparation of thymidine dimers having internucleosidic-3′5′)-methylene bonds. The latter procedure was utilized towards the synthesis, in solution and on a solid support, of DNA-fragments containing one or more T-CII2-T dimers. Further, 5′-O-methylthiomethyl-3′-O-methoxyacetyl-N 3-benzoyl-thymidine proved to be a suitable donor for the introduction of 5′-O-methylene acetal-linkage s between 2,3,4,6-tetra-Obenzyl-D-glucose, benzyl N-benzyloxycarbonyl-L-serine and dibenzyl phosphate.