DMT-dG(iPr-PAc)-CE-Phosphoramidite
N-[9-[(2R,4S,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-4-[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxyoxolan-2-yl]-6-oxo-1H-purin-2-yl]-2-(4-propan-2-ylphenoxy)acetamide
Product summary
Quick view
- Product family
- Oligonucleotide Synthesis, RNA Raw Materials & Modification
- Chemical Name
- N-[9-[(2R,4S,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-4-[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxyoxolan-2-yl]-6-oxo-1H-purin-2-yl]-2-(4-propan-2-ylphenoxy)acetamide
- MF
- C51H60N7O9P
- MW
- 946.0
- Purity
- 99.7% (NMR)
DMT-dG(iPr-PAc)-CE-Phosphoramidite is catalog CH70389, with CAS 150065-82-0, molecular formula C51H60N7O9P, molecular weight 946.0, and PubChem CID 136670604. PubChem lists InChIKey BTWWAYGTCZANKL-JIRGUTPESA-N for this identity.
A protected CE phosphoramidite reference for identifying this modified nucleoside monomer in oligonucleotide synthesis catalogs.
Identity and specifications
| Catalog No. | CH70389 |
| Product Name | DMT-dG(iPr-PAc)-CE-Phosphoramidite |
| CAS No. | 150065-82-0 |
| PubChem CID | 136670604 |
| Molecular Formula | C51H60N7O9P |
| Molecular Weight | 946.0 |
| Exact Mass | 945.41901351 |
| Monoisotopic Mass | 945.41901351 |
| InChIKey | BTWWAYGTCZANKL-JIRGUTPESA-N |
| Structural Note | protected nucleoside CE phosphoramidite identity |
| Purity | 99.7% (NMR) |
Storage conditions
at or below -20 C
Technical attributes
- Monomer class
- DNA CE phosphoramidite
- Nucleobase
- Guanine
- 5'-O protection
- DMT
- Base protection
- N2-(4-isopropylphenoxyacetyl)
- Grade
- Standard
- Packaging
- 1 g / ABI 15 mL / 20 mm septum; 1 g / ABI 60 mL / 20 mm septum; 1 g / Expedite 30 mL / 18 mm; 1 g / MerMade 30 mL / 28-400; 2 g / MerMade 30 mL / 28-400; 20 mL amber bottle with serum-vial neck; Custom packaging on request
- Water content
- 0.0%
- Physical form
- Powder
- Stability
- Phosphoramidite solutions: use within 24 h
Application context
- DMT-dG(iPr-PAc)-CE-Phosphoramidite reference: use this CE phosphoramidite monomer record for oligonucleotide synthesis monomer catalog work.
- Identifier cross-check: compare CAS 150065-82-0, PubChem CID 136670604, formula C51H60N7O9P, MW 946.0, and the listed InChIKey for catalog identity matching.
- Inquiry preparation: include catalog number CH70389, the product name, and the identity-matching identifiers when preparing a CHEMOS product inquiry.
Additional material information
Uses
Use these identifiers to match DMT-dG(iPr-PAc)-CE-Phosphoramidite against catalog records, PubChem references, and research-use product records.
Characteristics
DMT-dG(iPr-PAc)-CE-Phosphoramidite is presented as a protected nucleoside CE phosphoramidite identity with CAS 150065-82-0, PubChem CID 136670604, molecular formula C51H60N7O9P, molecular weight 946.0, and InChIKey BTWWAYGTCZANKL-JIRGUTPESA-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 136670604
PubChem · CID 136670604
Frequently Asked Questions
What is DMT-dG(iPr-PAc)-CE-Phosphoramidite?
DMT-dG(iPr-PAc)-CE-Phosphoramidite is catalog CH70389. PubChem lists CID 136670604, molecular formula C51H60N7O9P, molecular weight 946.0, and the InChIKey shown in the specification table.
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