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| 2,3-Dibromofuran-5-carboxylic acid Basic information |
Product Name: | 2,3-Dibromofuran-5-carboxylic acid | Synonyms: | 4,5-DIBROMO-2-FUROIC ACID;2,3-DIBROMOFURAN-5-CARBOXYLIC ACID;4,5-Dibromo-2-furancarboxylic acid;4,5-Dibromo-2-furoicacid,97%;4,5-DibroMo-2-furoic acid 97%;2-Furancarboxylic acid, 4,5-dibromo-;4,5-dibromofuran-2-carboxylic acid | CAS: | 2434-03-9 | MF: | C5H2Br2O3 | MW: | 269.88 | EINECS: | | Product Categories: | Building Blocks;C4 to C7;C4 to C8;Chemical Synthesis;Furans;Halogenated Heterocycles;Heterocyclic Building Blocks;Heterocycles | Mol File: | 2434-03-9.mol | |
| 2,3-Dibromofuran-5-carboxylic acid Chemical Properties |
Melting point | 169-173 °C | Boiling point | 328.7±42.0 °C(Predicted) | density | 2.304±0.06 g/cm3(Predicted) | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | pka | 2.58±0.16(Predicted) | BRN | 129312 | CAS DataBase Reference | 2434-03-9(CAS DataBase Reference) |
Hazard Codes | Xn | Risk Statements | 22-36/37/38 | Safety Statements | 26-36 | WGK Germany | 3 | HS Code | 2932190090 |
| 2,3-Dibromofuran-5-carboxylic acid Usage And Synthesis |
Uses | 2,3-Dibromofuran-5-carboxylic acid is used in a study of the effect of a furanyl halo-substituent on the intramolecular Diels-Alder reaction between the furan ring system and a pendant allylamide. The yield of the cycloaddition is improved with a C-5 bromide vs -chloro or -unsubstituted furan. |
| 2,3-Dibromofuran-5-carboxylic acid Preparation Products And Raw materials |
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