2-(2-azanylpurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
2-aminopurine riboside
CAS: 4546-54-7
Molecular Formula: C10H13N5O4
2-(2-azanylpurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol - Names and Identifiers
| Name | 2-aminopurine riboside |
| Synonyms | 2-AMINOPURINE RIBOSIDE 2-aminopurine riboside 2-Amino-9--D-ribofuranosylpurine 2-Amino-9-b-D-ribofuranosylpurine 9-pentofuranosyl-9H-purin-2-amine 2-AMINO-9-(BETA-D-RIBOFURANOSYL)PURINE 2-Amino-9-beta-D-ribofuranosyl-9H-purine 2-(2-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol 2-(2-azanylpurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol 2-(2-aminopurin-9-yl)-5-methylol-tetrahydrofuran-3,4-diol |
| CAS | 4546-54-7 |
| EINECS | 1312995-182-4 |
| InChI | InChI=1/C10H13N5O4/c11-10-12-1-4-8(14-10)15(3-13-4)9-7(18)6(17)5(2-16)19-9/h1,3,5-7,9,16-18H,2H2,(H2,11,12,14) |
2-(2-azanylpurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol - Physico-chemical Properties
| Molecular Formula | C10H13N5O4 |
| Molar Mass | 267.24 |
| Density | 2.08g/cm3 |
| Melting Point | 105-115°C |
| Boling Point | 711.8°C at 760 mmHg |
| Flash Point | 384.3°C |
| Solubility | DMSO (Slightly), Methanol (Slightly, Heated), Water (Slightly) |
| Vapor Presure | 2.88E-21mmHg at 25°C |
| Appearance | Solid |
| Color | White to Off-White |
| Storage Condition | -20°C Freezer |
| Refractive Index | 1.907 |
2-(2-azanylpurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol - Introduction
2-aminopurine riboside(2-aminopurine riboside) is an organic compound with the formula C10H12N4O4. It consists of 2-aminopurine and a ribosyl group.
2-aminopurine riboside can be used as a building block for RNA and DNA in organisms. It is often used as a fluorine probe or marker for DNA and RNA in biological research to study nucleic acid structure and function. Since 2-aminopurine is structurally similar to adenine, 2-aminopurine riboside can also be used in place of adenine in some cases.
The preparation method of 2-aminopurine riboside generally involves a chemical synthesis method using nucleotide synthesis. Specifically, 2-aminopurine riboside can be generated by chemical reaction of protecting groups of nucleotides.
Regarding the safety information of 2-aminopurine riboside, due to the lack of relevant studies and data, there is no specific safety evaluation. Appropriate safety practices and personal protective measures should be followed when using chemicals in any laboratory. Try to avoid contact with skin, eyes and mucous membranes, and ensure that the operation is carried out in a well-ventilated environment. If you come into contact with this compound, rinse immediately with plenty of water and seek medical attention.
2-aminopurine riboside can be used as a building block for RNA and DNA in organisms. It is often used as a fluorine probe or marker for DNA and RNA in biological research to study nucleic acid structure and function. Since 2-aminopurine is structurally similar to adenine, 2-aminopurine riboside can also be used in place of adenine in some cases.
The preparation method of 2-aminopurine riboside generally involves a chemical synthesis method using nucleotide synthesis. Specifically, 2-aminopurine riboside can be generated by chemical reaction of protecting groups of nucleotides.
Regarding the safety information of 2-aminopurine riboside, due to the lack of relevant studies and data, there is no specific safety evaluation. Appropriate safety practices and personal protective measures should be followed when using chemicals in any laboratory. Try to avoid contact with skin, eyes and mucous membranes, and ensure that the operation is carried out in a well-ventilated environment. If you come into contact with this compound, rinse immediately with plenty of water and seek medical attention.
Last Update：2024-04-10 22:29:15
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