129399-18-4

Basic information

• Product Name: N²-isobutyryl-7-<(2α,4R,5R)-4-<(benzoyloxy)methyl>-5-2-(hydroxyethyl)tetrahydrofuran-2-yl>guanine
• CAS NO: 129399-18-4
• Molecular Weight: 469.497
• Mol File: 129399-18-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N²-isobutyryl-7-<(2α,4R,5R)-4-<(benzoyloxy)methyl>-5-2-(hydroxyethyl)tetrahydrofuran-2-yl>guanine(CAS DataBase Reference)
• NIST Chemistry Reference: N²-isobutyryl-7-<(2α,4R,5R)-4-<(benzoyloxy)methyl>-5-2-(hydroxyethyl)tetrahydrofuran-2-yl>guanine(129399-18-4)
• EPA Substance Registry System: N²-isobutyryl-7-<(2α,4R,5R)-4-<(benzoyloxy)methyl>-5-2-(hydroxyethyl)tetrahydrofuran-2-yl>guanine(129399-18-4)

Safety Data

• Hazardous Substances Data: 129399-18-4(Hazardous Substances Data)

Upstream product

• 134056-30-7 3-deoxy-3-<(benzoyloxy)-methyl>-5,6-bis-O-(methylsulfonyl)-1,2-O-isopropylidene-α-D-allofuranose 
• 134056-17-0 (1R,5R,6R,7R)-6-<(benzoyloxy)methyl>-7-<<3-(trifluoromethyl)benzoyl>oxy>-2,8-dioxabicyclo<3.2.1>octane 
• 134056-14-7 3,5-dideoxy-3-<(benzoyloxy)methyl>-1,2-O-isopropylidene-α-D-allofuranose 
• 134056-13-6 3,5,6-trideoxy-5,6-didehydro-3-<(benzoyloxy)-methyl>-1,2-O-isopropylidene-α-D-allofuranose 
• 441044-21-9 Benzoic acid (2R,3S,4R)-4-hydroxy-2-(2-hydroxy-ethyl)-5-methoxy-tetrahydro-furan-3-ylmethyl ester 
• 134056-16-9 (1R,5R,6R,7R)-6-<(benzoyloxy)methyl>-7-hydroxy-2,8-dioxabicyclo<3.2.1>octane 
• 98-88-4 benzoyl chloride 
• 130469-40-8 3-deoxy-3-<(benzoyloxy)methyl>-1,2:5,6-di-O-isopropylidene-α-D-allofuranose 
• 130495-83-9 3-deoxy-3-<(benzoyloxy)methyl>-1,2-O-isopropylidene-α-D-allofuranose 
• 128435-09-6 (2RS,4R,5R)-2-methoxy-4-<(4-pivaloyloxy)methyl>-5-(2-hydroxyethyl)-tetrahydrofuran 
• 129518-74-7 (1R,5R,6R)-6-<(pivaloyloxy)methyl>-2,8-dioxabicyclo-<3.2.1>octane 
• 134056-12-5 (1R,5R,6R)-6-(hydroxymethyl)-2,8-dioxabicyclo-<3.2.1>octane 
• 69832-48-0 ((3aR,5S,6R,6aR)-tetrahydro-2,2-dimethyl-5-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)furo[2,3-d][1,3]dioxol-6-yl)methanol 
• 129399-08-2 (1R,5R,6R)-6-<(benzoyloxy)methyl>-2,8-dioxabicyclo-<3.2.1>octane 

Relevant articles and documents

Building Blocks for Oligonucleotide Analogues with Dimethylene Sulfide, Sulfoxide, and Sulfone Groups Replacing Phosphodiester Linkages

Two routes are presented for the synthesis of 3',5'-bishomodeoxyribonucleosides, building blocks needed to synthesize oligodeoxynucleotide analogues where the OPO2O groups are replaced by CH2SCH2, CH2SOCH2, and CH2SO2CH2 units.Two of these have been coupl