1,2,3,4-Tetra-o-acetyl-ß-D-glucopyranuronate structure 
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        Common Name | 1,2,3,4-Tetra-o-acetyl-ß-D-glucopyranuronate | ||
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| CAS Number | 7355-18-2 | Molecular Weight | 376.31 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 412.3±45.0 °C at 760 mmHg | |
| Molecular Formula | C15H20O11 | Melting Point | 179 °C | |
| MSDS | Chinese USA | Flash Point | 178.4±28.8 °C | |
            Use of 1,2,3,4-Tetra-o-acetyl-ß-D-glucopyranuronateMethyl tetra-O-acetyl-β-D-glucopyranuronate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.  | 
    
| Name | 1,2,3,4-Tetra-O-acetyl-β-D-glucuronic Acid Methyl Ester | 
|---|---|
| Synonym | More Synonyms | 
| Description | Methyl tetra-O-acetyl-β-D-glucopyranuronate is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | 
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| Related Catalog | 
| Density | 1.3±0.1 g/cm3 | 
|---|---|
| Boiling Point | 412.3±45.0 °C at 760 mmHg | 
| Melting Point | 179 °C | 
| Molecular Formula | C15H20O11 | 
| Molecular Weight | 376.31 | 
| Flash Point | 178.4±28.8 °C | 
| Exact Mass | 376.100555 | 
| PSA | 140.73000 | 
| LogP | 1.88 | 
| Vapour Pressure | 0.0±1.0 mmHg at 25°C | 
| Index of Refraction | 1.482 | 
| Storage condition | 2-8°C | 
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter | 
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| Hazard Codes | Xi | 
| RIDADR | NONH for all modes of transport | 
| WGK Germany | 3 | 
| Precursor 9 | |
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| DownStream 10 | |
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                                    Design and synthesis of water-soluble glucuronide derivatives of camptothecin for cancer prodrug monotherapy and antibody-directed enzyme prodrug therapy (ADEPT).
                                    
                                    
                                     J. Med. Chem. 42 , 3623-8, (1999) Glucuronide prodrugs of 9-aminocamptothecin were synthesized. Prodrug 4, in which 9-aminocamptothecin was connected to glucuronic acid by an aromatic spacer via a carbamate linkage, was stable in both...  | 
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                                    Synthesis and role of glycosylthio heterocycles in carbohydrate chemistry Ashry, E., et al.
                                    
                                    
                                     Tetrahedron 62 , 2943-98, (2006) 
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| T6OTJ BVO1 COV1 DOV1 EOV1 FOV1 &&β-D-Gluco Form | 
| 1,2,3,4-Tetra-o-acetyl-ß-D-glucopyranuronate | 
| Methyl 3,4,5,6-tetra(acetyloxy)tetrahydro-2H-pyran-2-carboxylate | 
| Methyl 1,2,3,4-tetra-O-acetyl-β-D-glucopyranuronate | 
| Methyl O-tetraacetyl-β-D-glucopyranuronate | 
| Methyl 1,2,3,4-Tetra-O-acetyl-β-D-glucuronate | 
| EINECS 230-880-3 | 
| β-D-Glucopyranuronic acid, methyl ester, 1,2,3,4-tetraacetate | 
| β-D-Glucopyranuronic acid, methyl ester, tetraacetate | 
| MFCD00069834 |