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2',3'-O-Isopropylideneadenosine, 98%, Thermo Scientific Chemicals
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Catalog number H53401.06
also known as H53401-06
Price (USD)/ Each
61.40
-
Quantity:
5 g
Price (USD)/ Each
61.40
2',3'-O-Isopropylideneadenosine, 98%, Thermo Scientific Chemicals
Catalog numberH53401.06
Price (USD)/ Each
61.40
-
Chemical Identifiers
CAS362-75-4
IUPAC Name[(3aR,4R,6R,6aR)-6-(6-amino-9H-purin-9-yl)-2,2-dimethyl-tetrahydro-2H-furo[3,4-d][1,3]dioxol-4-yl]methanol
Molecular FormulaC13H17N5O4
InChI KeyLCCLUOXEZAHUNS-AUWRGFAENA-N
SMILESCC1(C)O[C@@H]2[C@@H](CO)O[C@H]([C@@H]2O1)N1C=NC2=C(N)N=CN=C12
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Specifications
Specification Sheet
Specification SheetAssay (HPLC)97.5% min
2',3'-O-Isopropylideneadenosine is used as an organic chemical synthesis intermediate.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2′,3′-O-Isopropylideneadenosine is used as an organic chemical synthesis intermediate.
Notes
Stable under recommended storage conditions. Store away from oxidizing agents.
2′,3′-O-Isopropylideneadenosine is used as an organic chemical synthesis intermediate.
Notes
Stable under recommended storage conditions. Store away from oxidizing agents.
RUO – Research Use Only
General References:
- Peter J.Harper; Alexander Hampton. Conversion of 2',3'-O-isopropylideneadenosine into the 5',5'-di-C-methyl derivative. J. Org. Chem. 1970, 35, (5),1688-1689
- Kentaro Anzai; Jun Uzawa. Cyclonucleoside formation and ring cleavage in the reaction of 2',3'-O-isopropylideneadenosine with benzoyl chloride and its substituted derivatives. J. Org. Chem. 1984, 49, (26),5076-5080