A nucleoside building block
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N6-benzoyl-2'-Deoxyadenosine

Item No. 30262

Technical Information
Formal Name
N-benzoyl-2′-deoxy-adenosine
CAS Number
4546-72-9
Synonyms
  • N-Benzoyldeoxyadenosine
  • 6-N-Benzoyldeoxyadenosine
Molecular Formula
C17H17N5O4
Formula Weight
Purity
≥95%
A crystalline solid
DMF: 30 mg/mlDMF:PBS (pH 7.2) (1:6): 0.14 mg/mlDMSO: 15 mg/mlEthanol: 1 mg/ml
λmax
281 nm
SMILES
[H][C@@]1(C[C@H](O)[C@@H](CO)O1)N2C3=NC=NC(NC(C4=CC=CC=C4)=O)=C3N=C2
InChi Code
InChI=1S/C17H17N5O4/c23-7-12-11(24)6-13(26-12)22-9-20-14-15(18-8-19-16(14)22)21-17(25)10-4-2-1-3-5-10/h1-5,8-9,11-13,23-24H,6-7H2,(H,18,19,21,25)/t11-,12+,13+/m0/s1
InChi Key
PIXHJAPVPCVZSV-YNEHKIRRSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    N6-benzoyl-2'-Deoxyadenosine is a nucleoside building block.1,2 It is amino-protected and has been used in the synthesis of various oligonucleotides.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Mishra, R.K., and Misra, K. Improved synthesis of oligodeoxyribonucleotide using 3-methoxy-4-phenoxybenzoyl group for amino protection. Nucleic Acids Res. 14(15), 6197-6213 (1986).

    2. Garcia, J., Fernández, S., Ferrero, M., et alBuilding blocks for the solution phase synthesis of oligonucleotides: Regioselective hydrolysis of 3',5'-Di-O-levulinylnucleosides using an enzymatic approach. The Journal of Organic Chemistry 67(13), 4513-4519 (2002).