Decitabine Impurity 1 (alpha-Isomer)
Methyl-2-deoxy-alpha-D-ribofuranoside
CAS: 51255-17-5
Molecular Formula: C6H12O4
Decitabine Impurity 1 (alpha-Isomer) - Names and Identifiers
| Name | Methyl-2-deoxy-alpha-D-ribofuranoside |
| Synonyms | METHYL 2-DEOXY-D-RIBOSIDE A-D-ERYTHRO-PENTOFURANOSIDE Methyl-2-deoxy-alpha-D-ribofur ALPHA-D-ERYTHRO-PENTOFURANOSIDE Methyl-2-deoxy-α-D-Ribofuranoside Methyl 2-deoxy-a-D-ribofuranoside Decitabine Impurity 1 (alpha-Isomer) METHYL-2-DEOXY-ALPHA-D-RIBOFURANOSIDE Methyl-2-deoxy-alpha-D-ribofuranoside α-D-erythro-Pentofuranoside, methyl 2-deoxy- |
| CAS | 51255-17-5 |
| InChI | InChI=1/C6H11O4/c1-9-4-2-6(8)10-5(4)3-7/h4-7H,2-3H2,1H3/q-1/t4-,5+,6-/m0/s1 |
Decitabine Impurity 1 (alpha-Isomer) - Physico-chemical Properties
| Molecular Formula | C6H12O4 |
| Molar Mass | 148.16 |
| Density | 1.24±0.1 g/cm3(Predicted) |
| Boling Point | 294.5±40.0 °C(Predicted) |
| pKa | 13.81±0.60(Predicted) |
| Refractive Index | 1.487 |
Decitabine Impurity 1 (alpha-Isomer) - Introduction
Methyl-2-deoxy-alpha-D-ribofuranoside is a nucleoside compound, which is named after the methyl group forms a chemical bond with 2-deoxy-alpha-D-ribofuranose. Its molecular formula is C11H20N2O5 and its relative molecular mass is 260.29g/mol.
Methyl-2-deoxy-alpha-D-ribofuranoside is a white or slightly yellow crystalline powder at room temperature, soluble in solvents such as water, methanol and chloroform. It is an unstable compound that decomposes under conditions of prolonged storage or heating. It has chemical properties similar to nucleosides and can be involved in the generation and modification of nucleic acids.
Methyl-2-deoxy-alpha-D-ribofuranoside have important applications in biochemistry and pharmaceuticals. It can be used for synthetic drugs, DNA modification and nucleic acid sequence analysis and other related research. It is also used as a chemical reagent in the laboratory for the synthesis and study of nucleic acid-related compounds.
The method for preparing Methyl-2-deoxy-alpha-D-ribofuranoside is mainly obtained by chemical synthesis of nucleosides. A common synthetic method is to introduce a methyl group to the 2-hydroxyl group of ribose by reacting a riboside compound with a methylating agent to obtain Methyl-2-deoxy-alpha-D-ribofuranoside.
There are no specific toxicity or danger reports regarding the safety of the Methyl-2-deoxy-alpha-D-ribofuranoside. However, because it has not been widely studied and applied, its specific toxicology and safety still need further research and evaluation. When using and handling, it is recommended to follow good laboratory practices, avoid direct contact and inhalation, avoid accidental ingestion, and correct storage and disposal.
Methyl-2-deoxy-alpha-D-ribofuranoside is a white or slightly yellow crystalline powder at room temperature, soluble in solvents such as water, methanol and chloroform. It is an unstable compound that decomposes under conditions of prolonged storage or heating. It has chemical properties similar to nucleosides and can be involved in the generation and modification of nucleic acids.
Methyl-2-deoxy-alpha-D-ribofuranoside have important applications in biochemistry and pharmaceuticals. It can be used for synthetic drugs, DNA modification and nucleic acid sequence analysis and other related research. It is also used as a chemical reagent in the laboratory for the synthesis and study of nucleic acid-related compounds.
The method for preparing Methyl-2-deoxy-alpha-D-ribofuranoside is mainly obtained by chemical synthesis of nucleosides. A common synthetic method is to introduce a methyl group to the 2-hydroxyl group of ribose by reacting a riboside compound with a methylating agent to obtain Methyl-2-deoxy-alpha-D-ribofuranoside.
There are no specific toxicity or danger reports regarding the safety of the Methyl-2-deoxy-alpha-D-ribofuranoside. However, because it has not been widely studied and applied, its specific toxicology and safety still need further research and evaluation. When using and handling, it is recommended to follow good laboratory practices, avoid direct contact and inhalation, avoid accidental ingestion, and correct storage and disposal.
Last Update：2024-04-09 21:54:55
