Modified Nucleosides
N2-Isobutyryl-3'-O-methylguanosine
Quick view. An N2-isobutyryl-protected 3'-O-methylguanosine building block for structure-specific modified-nucleoside and nucleotide synthesis research. CAS 160107-07-3. Catalog target purity: By inquiry. Availability: Inquiry only — contact OROGO to confirm current availability.
Request a quote Review request checklist
Product profile
N2-Isobutyryl-3'-O-methylguanosine is classified as modified nucleosides (Formula C15H21N5O6; molecular weight 367.36).
N2-Isobutyryl-3'-O-methylguanosine — N2-isobutyryl-protected 3'-O-methylguanosine building block for structure-specific modified-nucleoside and nucleotide synthesis research.
For N2-Isobutyryl-3'-O-methylguanosine, the 3′-O-methyl group blocks normal 3′-hydroxyl extension; confirm that this behavior matches the intended enzyme or synthesis workflow.
Names and search terms
Confirmed or normalized name variants
- N2-iso-Butyroyl-3'-O-methylguanosine
Useful catalog search terms
- CAS 160107-07-3
- PubChem CID 145710473
Physicochemical data
| PubChem CID | 145710473 |
|---|---|
| InChIKey | WKXJLMCHKRMCEY-AKAIJSEGSA-N |
| IUPAC name | N-[9-[(2R,3R,4S,5R)-3-hydroxy-5-(hydroxymethyl)-4-methoxyoxolan-2-yl]-6-oxo-1H-purin-2-yl]-2-methylpropanamide |
| SMILES | CC(C)C(=O)NC1=NC2=C(C(=O)N1)N=CN2[C@H]3[C@@H]([C@@H]([C@H](O3)CO)OC)O |
| Base protection | N2-isobutyryl |
| Sugar modification | 3'-O-methyl |
| InChI | InChI=1S/C15H21N5O6/c1-6(2)12(23)18-15-17-11-8(13(24)19-15)16-5-20(11)14-9(22)10(25-3)7(4-21)26-14/h5-7,9-10,14,21-22H,4H2,1-3H3,(H2,17,18,19,23,24)/t7-,9-,10-,14-/m1/s1 |
Release documentation
The current specification defines the analytical method and acceptance criteria; the released lot result is reported on the CoA.
Additional HPLC, MS or NMR documentation can be agreed during technical review where available.
Product-specific evaluation notes
Potential advantages
- 3′-O-methylation provides a defined blocked ribose terminus and is analytically distinguishable from the corresponding 2′-O-methyl isomer.
Method limitations
- The 3′-O-methyl group blocks normal 3′-hydroxyl extension; confirm that this behavior matches the intended enzyme or synthesis workflow.
These points describe N2-Isobutyryl-3'-O-methylguanosine or its named chemical feature. Broader product-family guidance is maintained on the category page.
Related products
(S)-cEt-rA
Modified Nucleosides · CAS: 1197033-34-3
OR-OP-0069S-Adenosyl-L-methionine (SAM)
Modified Nucleosides · CAS: 485-80-3
OR-MN-01875-(Carboxyhydroxymethyl)uridine
Modified Nucleosides · CAS: 934743-11-0
OR-MN-0719(R)-N6-(2,3-Dihydro-1H-inden-1-yl)adenosine
Modified Nucleosides · CAS: 96392-15-3
OR-MN-01972,2'-Cyclocytidine hydrochloride
Modified Nucleosides · CAS: 10212-25-6
OR-MN-0199N3-Allyluridine
Modified Nucleosides · CAS: 103951-13-9
Product-family literature
These publications provide peer-reviewed context for the Modified Nucleosides product family and its named chemistry. They are background reading only, not evidence for the exact product, supplied form, lot specification, availability or performance.
Request a quote Review request checklist
Technology platforms
Catalog-derived platform membership for navigating related chemistry and verifiable product sets.
