N6-Benzoyl-2'-O,4'-C-methylene-adenosine
N-[9-[(1S,3R,4R,7S)-7-hydroxy-1-(hydroxymethyl)-2,5-dioxabicyclo[2.2.1]heptan-3-yl]purin-6-yl]benzamide
Product summary
Quick view
- Product family
- Oligonucleotide Synthesis, RNA Raw Materials & Modification
- Chemical Name
- N-[9-[(1S,3R,4R,7S)-7-hydroxy-1-(hydroxymethyl)-2,5-dioxabicyclo[2.2.1]heptan-3-yl]purin-6-yl]benzamide
- MF
- C18H17N5O5
- MW
- 383.4
- Purity
- 99.98%
N6-Benzoyl-2'-O,4'-C-methylene-adenosine is catalog CH70155, with CAS 209968-94-5, molecular formula C18H17N5O5, molecular weight 383.4, and PubChem CID 11069003. PubChem lists InChIKey LWLHBOKWFIOXPA-OBQMCUGOSA-N for this identity.
A modified nucleoside reference for nucleic-acid chemistry catalog search and structure matching.
Identity and specifications
| Catalog No. | CH70155 |
| Product Name | N6-Benzoyl-2'-O,4'-C-methylene-adenosine |
| CAS No. | 209968-94-5 |
| PubChem CID | 11069003 |
| Molecular Formula | C18H17N5O5 |
| Molecular Weight | 383.4 |
| Exact Mass | 383.12296866 |
| Monoisotopic Mass | 383.12296866 |
| InChIKey | LWLHBOKWFIOXPA-OBQMCUGOSA-N |
| Structural Note | modified nucleoside identity |
| Purity | 99.98% |
Storage conditions
Powder -20 C; in solvent -80 C
Technical attributes
- Material class
- Protected LNA nucleoside
- Nucleobase
- Adenine
- Sugar bridge
- 2'-O,4'-C-methylene
- Base protection
- N6-benzoyl
- Packaging
- 10 mg; 50 mg; 1 g; 10 g; 100 g; 1 kg; 5 kg; Custom packaging on request
- Stability
- Powder 3 years at -20 C; in solvent 1 year at -80 C
Application context
- N6-Benzoyl-2'-O,4'-C-methylene-adenosine reference: use this modified nucleoside building block record for nucleic-acid chemistry catalog work.
- Identifier cross-check: compare CAS 209968-94-5, PubChem CID 11069003, formula C18H17N5O5, MW 383.4, and the listed InChIKey for catalog identity matching.
- Inquiry preparation: include catalog number CH70155, the product name, and the identity-matching identifiers when preparing a CHEMOS product inquiry.
Additional material information
Uses
Use these identifiers to match N6-Benzoyl-2'-O,4'-C-methylene-adenosine against catalog records, PubChem references, and research-use product records.
Characteristics
N6-Benzoyl-2'-O,4'-C-methylene-adenosine is presented as a modified nucleoside identity with CAS 209968-94-5, PubChem CID 11069003, molecular formula C18H17N5O5, molecular weight 383.4, and InChIKey LWLHBOKWFIOXPA-OBQMCUGOSA-N.
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 11069003
PubChem · CID 11069003
Frequently Asked Questions
What is N6-Benzoyl-2'-O,4'-C-methylene-adenosine?
N6-Benzoyl-2'-O,4'-C-methylene-adenosine is catalog CH70155. PubChem lists CID 11069003, molecular formula C18H17N5O5, molecular weight 383.4, and the InChIKey shown in the specification table.
Similar Products
Need Help with Material Selection?
CHEMOS can review product fit, target structure, route questions, analytical expectations, and project-specific supply needs.