1174917-95-3

Basic information

• Product Name: C₃₈H₄₆O₈SSi
• Synonyms: C₃₈H₄₆O₈SSi
• CAS NO: 1174917-95-3
• Molecular Weight: 690.93
• Mol File: 1174917-95-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: C₃₈H₄₆O₈SSi(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₈H₄₆O₈SSi(1174917-95-3)
• EPA Substance Registry System: C₃₈H₄₆O₈SSi(1174917-95-3)

Safety Data

• Hazardous Substances Data: 1174917-95-3(Hazardous Substances Data)

Upstream product

• 1093849-11-6 C₃₇H₄₂O₆Si 
• 1070968-94-3 C₂₀H₂₄O₆ 
• 956485-08-8 ((3aR,5R,6S,6aR)-5-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethyl-6-(naphthalen-2-ylmethoxy)tetrahydrofuro[2,3-d][1,3]dioxol-5-yl)methanol 
• 956485-07-7 ((3aR,6S,6aR)-2,2-dimethyl-6-(naphthalen-2-ylmethoxy)tetrahydrofuro[3,2-d][1,3]dioxole-5,5-diyl)dimethanol 
• 1057385-93-9 (3aR,5S,6R,6aR)-2,2-dimethyl-6-(naphthalen-2-ylmethoxy)tetrahydrofuro[3,2-d][1,3]dioxole-5-carbaldehyde 
• 620630-82-2 1,2 5,6-O-di(isopropylidene)-α-D-allofuranose 
• 939-26-4 2-bromomethylnaphthyl bromide 
• 124-63-0 methanesulfonyl chloride 

Downstream Products

• 1174917-96-4 1,2-di-O-acetyl-5-O-(tert-butyldiphenylsilyl)-4-C-((1S)-1-methanesulfonyloxyethyl)-3-O-(2-naphthylmethyl)-D-ribofuranose 
• 1352231-54-9 C₃₄H₃₇N₃O₇ 
• 1352229-98-1 C₄₀H₄₆N₂O₉SSi 
• 1352230-05-7 C₄₁H₄₅F₃N₂O₁₁S₂Si 
• 1352231-52-7 C₄₀H₄₅N₃O₅Si 
• 1352231-50-5 C₄₀H₄₆N₂O₉SSi 
• 1232328-95-8 C₄₂H₄₈N₂O₁₀SSi 
• 1352231-59-4 C₄₁H₄₈N₂O₁₁S₂Si 
• 1352230-09-1 C₃₉H₄₂N₂O₅SSi 
• 1352230-52-4 C₂₈H₃₄N₂O₅SSi 
• 1352230-53-5 C₃₃H₃₄N₂O₇S 
• 1352230-16-0 C₄₂H₅₁N₄O₈PS 
• 1352230-54-6 C₃₉H₄₈N₂O₇SSi 

Relevant articles and documents

BICYCLIC MORPHOLINO COMPOUNDS AND OLIGOMERIC COMPOUNDS PREPARED THEREFROM

The present invention provides bicyclic morpholino compounds and oligomeric compounds prepared therefrom. More particularly, incorporation of one or more of the bicyclic morpholino compounds into an oligomeric compound is expected to enhance one or more p

Synthesis and biophysical evaluation of 2′,4′-Constrained 2′O-Methoxyethyl and 2′,4′-Constrained 2′O-Ethyl nucleic acid analogues

"Chemical Equation Presented" We have recently shown that combining the structural elements of 2′O-methoxyethyl (MOE) and locked nucleic acid (LNA) nucleosides yielded a series of nucleoside modifications (cMOE, 2′,4′-constrained MOE; cEt, 2′,4′-constrain