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| 2-Bromo-3′-hydroxyacetophenone Basic information |
Product Name: | 2-Bromo-3′-hydroxyacetophenone | Synonyms: | 2-Bromo-3'-hydroxyacetophenone, 2-Bromo-1-(3-hydroxyphenyl)ethan-1-one, 3-(Bromoacetyl)phenol;M-BroMoacetylphenol;omega-Bromo-m-hydroxyacetophenone;Ethanone,2-broMo-1-(3-hydroxyphenyl)-;2-bromo-1-(3-hydroxyphenyl)ethan-1-one;Phenylephrine Impurity 64;Carteolol Impurity 13;2-Bromo-3-Hydroxyacetophenone (2-Bromo-3-HAP) | CAS: | 2491-37-4 | MF: | C8H7BrO2 | MW: | 215.04 | EINECS: | | Product Categories: | Aromatics;Carbonyl Compounds;Ketones;C7 to C8 | Mol File: | 2491-37-4.mol | |
| 2-Bromo-3′-hydroxyacetophenone Chemical Properties |
Melting point | 70-74 °C(lit.) | Boiling point | 327.8±22.0 °C(Predicted) | density | 1.622±0.06 g/cm3(Predicted) | storage temp. | 2-8°C | solubility | soluble in Dichloromethane, Ethyl Acetate, Methanol | form | powder | pka | 8.97±0.10(Predicted) | color | Fawn to brown |
Hazard Codes | C | Risk Statements | 22-34-43 | Safety Statements | 26-36/37/39-45 | RIDADR | UN 3263 8/PG 2 | WGK Germany | 3 | HS Code | 29147000 |
| 2-Bromo-3′-hydroxyacetophenone Usage And Synthesis |
Chemical Properties | White Solid | Uses | Reactant involved in the synthesis of:
- Pyrrole-3-carboxylic acids
- N-aryl-N-thiazolyl compounds via the Hantzsch reaction
- Disubstituted oxadiazolylindole derivatives with antiinflammatory, analgesic and nitric oxide releasing activity
- Anilino-aryl-thiazoles with inhibitory activity toward valosin-containing proteins
- Tyrosine kinase erythropoietin inhibitors
- E. coli methionine aminopeptidase inhibitors
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| 2-Bromo-3′-hydroxyacetophenone Preparation Products And Raw materials |
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