5'-O-DMT-2'-FANA-2'-deoxy-N6-benzoyl-adenosine
N-[9-[(2R,3S,4R,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-3-fluoro-4-hydroxyoxolan-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)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-3-fluoro-4-hydroxyoxolan-2-yl]purin-6-yl]benzamide
- MF
- C38H34FN5O6
- MW
- 675.7
- Purity
- 97%
5'-O-DMT-2'-FANA-2'-deoxy-N6-benzoyl-adenosine is 5'-DMT N6-benzoyl 2'-FANA adenosine. Key identifiers include CAS 226415-08-3, molecular formula C38H34FN5O6, molecular weight 675.7, PubChem CID 67563215, and InChIKey DDOOVEXTSRBCMU-MHHBZGPPSA-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. | CH70310 |
| CAS No. | 226415-08-3 |
| Molecular Formula | C38H34FN5O6 |
| Molecular Weight | 675.7 |
| PubChem CID | 67563215 |
| InChIKey | DDOOVEXTSRBCMU-MHHBZGPPSA-N |
| Purity | 97% |
Storage conditions
2-8 C; dark place; inert atmosphere
Technical attributes
- Material class
- Protected 2'F-ANA nucleoside
- Nucleobase
- Adenine
- Sugar configuration
- 2'-Deoxy-2'-fluoro-arabino
- Protection pattern
- 5'-O-DMT; N6-benzoyl
- Packaging
- 50 mg; 100 mg; 250 mg; 1 g; Custom packaging on request
- Physical form
- Powder or crystals
Application context
- 5'-O-DMT-2'-FANA-2'-deoxy-N6-benzoyl-adenosine reference: use this 2'-fluoro arabino nucleoside building block record for modified oligonucleotide building-block review.
- Identifier cross-check: compare CAS 226415-08-3, PubChem CID 67563215, formula C38H34FN5O6, MW 675.7, and the listed InChIKey for catalog identity matching.
- Inquiry preparation: include catalog number CH70310, 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 67563215
PubChem · CID 67563215
Frequently Asked Questions
What is 5'-O-DMT-2'-FANA-2'-deoxy-N6-benzoyl-adenosine?
5'-O-DMT-2'-FANA-2'-deoxy-N6-benzoyl-adenosine is catalog CH70310, CAS 226415-08-3. PubChem CID 67563215 confirms formula C38H34FN5O6, molecular weight 675.7, and InChIKey DDOOVEXTSRBCMU-MHHBZGPPSA-N.
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