An intermediate in the synthesis of remdesivir
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Remdesivir O-desphosphate acetonide

Item No. 36673

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
2-C-(4-aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)-2,5-anhydro-3,4-O-(1-methylethylidene)-D-altrononitrile
CAS Number
1191237-80-5
Molecular Formula
C15H17N5O4
Formula Weight
331.3
Purity
≥98%
Formulation (Request formulation change)
A solid
Solubility(Learn about Variance in Solubility)
DMF: 12 mg/mlDMSO: 11 mg/mlEthanol: 5 mg/mlPBS (pH 7.2): 0.3 mg/ml
λmax
245 nm
SMILES
N#C[C@]1(C2=CC=C3N2N=CN=C3N)[C@@](OC(C)(C)O4)([H])[C@@]4([H])[C@@H](CO)O1
InChi Code
InChI=1S/C15H17N5O4/c1-14(2)23-11-9(5-21)22-15(6-16,12(11)24-14)10-4-3-8-13(17)18-7-19-20(8)10/h3-4,7,9,11-12,21H,5H2,1-2H3,(H2,17,18,19)/t9-,11-,12-,15+/m1/s1
InChi Key
IJCOKJGMVJGKBB-CGEWXTDFSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Remdesivir O-desphosphate acetonide is a synthetic intermediate in the synthesis of the antiviral prodrug remdesivir (Item No. 30354).1

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Gannedi, V., Villuri, B.K., Reddy, S.N., et al. Practical remdesivir synthesis through one-pot organocatalyzed asymmetric ( S)-P-phosphoramidation. The Journal of Organic Chemistry 86(7), 4977-4985 (2021).