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| | 2,3-Dimethoxybenzaldehyde Basic information |
| | 2,3-Dimethoxybenzaldehyde Chemical Properties |
| Melting point | 48-52 °C (lit.) | | Boiling point | 137 °C/12 mmHg (lit.) | | density | 1.1708 (rough estimate) | | refractive index | 1.5500 (estimate) | | Fp | >230 °F | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | Solubility in methanol with almost transparency. | | form | Crystalline Powder, Crystals, and/or Chunks | | color | Off-white to beige | | Sensitive | Air Sensitive | | BRN | 908264 | | InChI | 1S/C9H10O3/c1-11-8-5-3-4-7(6-10)9(8)12-2/h3-6H,1-2H3 | | InChIKey | JIVGSHFYXPRRSZ-UHFFFAOYSA-N | | SMILES | [H]C(=O)c1cccc(OC)c1OC | | LogP | 1.630 (est) | | CAS DataBase Reference | 86-51-1(CAS DataBase Reference) | | NIST Chemistry Reference | Benzaldehyde, 2,3-dimethoxy-(86-51-1) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 3 | | RTECS | CU5732000 | | Hazard Note | Irritant | | HS Code | 29124900 | | Storage Class | 11 - Combustible Solids |
| | 2,3-Dimethoxybenzaldehyde Usage And Synthesis |
| Description | 2,3-Dimethoxybenzaldehyde, commonly known as o-veratrol, is an important aromatic aldehyde compound. Its structure is characterized by two methoxy substituents and one aldehyde group at the ortho (2 and 3) positions of the benzene ring. Due to its unique chemical structure, this compound occupies a central position in the field of pharmaceutical intermediates, especially as a key precursor in the synthesis of berberine. Furthermore, it possesses significant biological activities, such as antifungal and antiviral effects. | | Chemical Properties | white to brown crystalline powder | | Uses | A benzaldehyde derivative that may possess antifungal activity of redox-active benzaldehydes that target cellular antioxidation. It could function as chemosensitizing agents in concert with convention
al drugs or fungicides to improve antifungal efficacy. | | Uses | 2,3-Dimethoxybenzaldehyde possess antifungal activity of redox-active benzaldehydes that target cellular antioxidation. It could function as chemosensitizing agents in concert with conventional drugs to improve antifungal efficacy. | | Safety Profile | A poison by ingestion.
When heated to decomposition it emits
acrid smoke and irritating vapors |
| | 2,3-Dimethoxybenzaldehyde Preparation Products And Raw materials |
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