7H-PYRROLO[2,3-D]PYRIMIDIN-4-OL
Pyrrolo[2,3-d]pyrimidin-4-ol
CAS: 3680-71-5
Molecular Formula: C6H5N3O
7H-PYRROLO[2,3-D]PYRIMIDIN-4-OL - Names and Identifiers
| Name | Pyrrolo[2,3-d]pyrimidin-4-ol |
| Synonyms | 7-DEAZAHYPOXANTHINE 7-DEAZA-6-HYDROXY PURINE Pyrrolo[2,3-d]pyrimidin-4-ol 1,7-Dihydro-pyrrolo[2,3-d... 7H-Pyrrolo[2,3-d]pyrimidin-4-ol 7H-PYRROLO[2,3-D]PYRIMIDIN-4-OL 4H-Pyrrolo[2,3-d]pyriMidin-4-one 4-HYDROXYPYRROLO[2,3-D]PYRIMIDINE 4-hydroxypyrrolo[2,3-d]pyrimidine 3H-PYRROLO[2,3-D]PYRIMIDIN-4(7H)-ONE 3H-pyrrolo[2,3-d]pyrimidin-4(7H)-one 1,7-DIHYDRO-4H-PYRROLO[3,2-D]PYRIMIDIN-4-ONE 1,7-dihydro-4H-pyrrolo[2,3-d]pyrimidin-4-one |
| CAS | 3680-71-5 |
| EINECS | 640-613-6 |
| InChI | InChI=1/C6H5N3O/c10-6-4-1-2-7-5(4)8-3-9-6/h1-3H,(H2,7,8,9,10) |
| InChIKey | FBMZEITWVNHWJW-UHFFFAOYSA-N |
7H-PYRROLO[2,3-D]PYRIMIDIN-4-OL - Physico-chemical Properties
| Molecular Formula | C6H5N3O |
| Molar Mass | 135.12 |
| Density | 1.62±0.1 g/cm3(Predicted) |
| Melting Point | 345-348°C |
| Boling Point | 473.1±18.0 °C(Predicted) |
| Flash Point | 191.4°C |
| Solubility | Soluble in dimethyl sulfoxide. |
| Vapor Presure | 2.22E-06mmHg at 25°C |
| Appearance | Crystalline powder |
| Color | Brown |
| pKa | 11.99±0.20(Predicted) |
| Storage Condition | 2-8°C |
| Sensitive | Moisture & Light Sensitive |
| Refractive Index | 1.784 |
| MDL | MFCD08234923 |
7H-PYRROLO[2,3-D]PYRIMIDIN-4-OL - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | R36 - Irritating to the eyes R43 - May cause sensitization by skin contact |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37 - Wear suitable protective clothing and gloves. |
| WGK Germany | 3 |
| RTECS | UY9440000 |
| HS Code | 29335990 |
| Hazard Class | IRRITANT |
7H-PYRROLO[2,3-D]PYRIMIDIN-4-OL - Reference Information
| Use | 4-hydroxypyrrolo [2,3-d] pyrimidine is a prodrug of xanthine oxidase activated thymidine phosphorylase inhibitor. 4-hydroxypyrrolido [2,3-d] pyrimidine is an organic synthesis and pharmaceutical intermediate. In the synthesis process of chemical medicine, it is mainly used to produce toffatinib, balectinib and other anticancer drugs. |
Last Update：2024-04-09 21:11:58
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