Sugars
1,2,3,5-Tetra-O-benzoyl-2-C-methyl-beta-D-ribofuranose
Quick view. A beta-D-ribofuranose derivative bearing a 2-C-methyl substituent and benzoyl protection at O-1, O-2, O-3, and O-5, CAS 30361-19-4. CAS 30361-19-4. Catalog target purity: By inquiry. Availability: Inquiry only — contact OROGO to confirm current availability.
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Product profile
1,2,3,5-Tetra-O-benzoyl-2-C-methyl-beta-D-ribofuranose is classified as sugars (Formula C34H28O9; molecular weight 580.60 g/mol).
1,2,3,5-Tetra-O-benzoyl-2-C-methyl-beta-D-ribofuranose — Benzoyl-protected 2-C-methyl-beta-D-ribofuranose building block for carbohydrate and nucleoside chemistry.
For 1,2,3,5-Tetra-O-benzoyl-2-C-methyl-beta-D-ribofuranose, confirm the current specification, storage conditions and downstream-method compatibility before routine use.
Names and search terms
Confirmed or normalized name variants
- 2-C-Methyl-1,2,3,5-tetra-O-benzoyl-beta-D-ribofuranose
- 2-C-Methyl-beta-D-ribofuranose 1,2,3,5-tetrabenzoate
Useful catalog search terms
- 30361-19-4
- PubChem CID 11813893
Physicochemical data
| PubChem CID | 11813893 |
|---|---|
| Anomer | beta-D-ribofuranose |
| Systematic name | (2R,3R,4R,5S)-4,5-bis(benzoyloxy)-2-[(benzoyloxy)methyl]-4-methyloxolan-3-yl benzoate |
| Protecting groups | O-benzoyl at positions 1, 2, 3, and 5 |
| Carbon substitution | 2-C-methyl |
| InChIKey | QJZSLTLDMBDKOU-OSVDXEOTSA-N |
| InChI | InChI=1S/C34H28O9/c1-34(43-32(38)26-20-12-5-13-21-26)28(41-30(36)24-16-8-3-9-17-24)27(22-39-29(35)23-14-6-2-7-15-23)40-33(34)42-31(37)25-18-10-4-11-19-25/h2-21,27-28,33H,22H2,1H3/t27-,28-,33?,34-/m1/s1 |
| SMILES | C[C@]1([C@@H]([C@H](OC1OC(=O)C2=CC=CC=C2)COC(=O)C3=CC=CC=C3)OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5 |
| Canonical SMILES | C[C@]1([C@@H]([C@H](OC1OC(=O)C2=CC=CC=C2)COC(=O)C3=CC=CC=C3)OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5 |
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.
Additional application examples
- Reference compound for chemical identity studies involving protected 2-C-methyl-beta-D-ribofuranose.
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