N6-Benzoyl-2'-FANA-2'-deoxyadenosine
N-[9-[(2R,3S,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]purin-6-yl]benzamide
Product summary
Quick view
- Product family
- Oligonucleotide Synthesis, RNA Raw Materials & Modification
- Chemical Name
- N-[9-[(2R,3S,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]purin-6-yl]benzamide
- MF
- C17H16FN5O4
- MW
- 373.3
- Purity
- 99.98%
N6-Benzoyl-2'-FANA-2'-deoxyadenosine is N6-benzoyl 2'-FANA adenosine. Key identifiers include CAS 144924-99-2, molecular formula C17H16FN5O4, molecular weight 373.3, PubChem CID 53883372, and InChIKey HLJZTLWDAQVZBU-WYFUGZQLSA-N.
The 2'F-ANA scaffold has an arabino 2'-fluoro sugar configuration. This page should present the item as a modified nucleoside or protected nucleoside identity reference, not as a CE phosphoramidite unless separate phosphoramidite evidence is supplied.
Identity and specifications
| Catalog No. | CH70152 |
| CAS No. | 144924-99-2 |
| Molecular Formula | C17H16FN5O4 |
| Molecular Weight | 373.3 |
| PubChem CID | 53883372 |
| InChIKey | HLJZTLWDAQVZBU-WYFUGZQLSA-N |
| Purity | 99.98% |
Storage conditions
Powder -20 C; in solvent -80 C
Technical attributes
- Material class
- Protected 2'F-ANA nucleoside
- Nucleobase
- Adenine
- Sugar configuration
- 2'-Deoxy-2'-fluoro-arabino
- Base protection
- N6-benzoyl
- Packaging
- 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg; 500 mg; 1 g; 5 g; 10 g; 25 g; 50 g; 100 g; 500 g; 1 kg; 10 kg; 100 kg; Custom packaging on request
- Stability
- Powder 3 years at -20 C; in solvent 1 year at -80 C
Application context
- N6-Benzoyl-2'-FANA-2'-deoxyadenosine reference: use this 2'-fluoro arabino nucleoside building block record for modified oligonucleotide building-block review.
- Identifier cross-check: compare CAS 144924-99-2, PubChem CID 53883372, formula C17H16FN5O4, MW 373.3, and the listed InChIKey for catalog identity matching.
- Inquiry preparation: include catalog number CH70152, the product name, and the identity-matching identifiers when preparing a CHEMOS product inquiry.
Related technical resources
Oligonucleotide Modification
Sugar, base, backbone, terminal, and conjugation modifications for ASO, siRNA, guide RNA, aptamer, and research or labeling oligo projects.
Oligonucleotide Synthesis
Support for modified monomers, supports, sulfurizing reagents, cap analogs, and related oligo synthesis inputs.
Public references
- Sustainability Challenges and Opportunities in Oligonucleotide Manufacturing
Journal of Organic Chemistry, 2021
Product-family technical context
- Solid-phase supports for oligonucleotide synthesis
Current Protocols in Nucleic Acid Chemistry, 2013
Product-family technical context
- Deoxynucleoside phosphoramidites—A new class of key intermediates for deoxypolynucleotide synthesis
Tetrahedron Letters, 1981
Product-family technical context
- Synthesis of deoxyoligonucleotides on a polymer support
Journal of the American Chemical Society, 1981
Product-family technical context
- PubChem Compound 53883372
PubChem · CID 53883372
Frequently Asked Questions
What is N6-Benzoyl-2'-FANA-2'-deoxyadenosine?
N6-Benzoyl-2'-FANA-2'-deoxyadenosine is catalog CH70152, CAS 144924-99-2. PubChem CID 53883372 confirms formula C17H16FN5O4, molecular weight 373.3, and InChIKey HLJZTLWDAQVZBU-WYFUGZQLSA-N.
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