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| | 5-Bromoindole-2-carboxylic acid Basic information |
| | 5-Bromoindole-2-carboxylic acid Chemical Properties |
| Melting point | 287-288 | | Boiling point | 470.9±25.0 °C(Predicted) | | density | 1.838±0.06 g/cm3(Predicted) | | storage temp. | -20°C | | pka | 4.25±0.30(Predicted) | | form | Solid | | color | White to Light yellow to Light orange | | InChI | InChI=1S/C9H6BrNO2/c10-6-1-2-7-5(3-6)4-8(11-7)9(12)13/h1-4,11H,(H,12,13) | | InChIKey | YAULOOYNCJDPPU-UHFFFAOYSA-N | | SMILES | N1C2=C(C=C(Br)C=C2)C=C1C(O)=O | | CAS DataBase Reference | 7254-19-5(CAS DataBase Reference) |
| | 5-Bromoindole-2-carboxylic acid Usage And Synthesis |
| Uses | Reactant involved in studies of biologically active molecules including:
- Discovery of indole inhibitors of MMP-13 for treatment of arthritic diseases
- Synthesis of indolyl ethanones as indoleamine 2,3-dioxygenase inhibitors
- cis-Diaminocyclohexane derivatives prepared for use as factor Xa inhibitors
- Synthesis of tubulin polymerization inhibitors and cancer cell growth inhibitors
- Preparation of dual PPARγ/δ agonists
- Synthesis of chemical probes to examine the role of hFPRL1 receptor in inflammation
| | Uses | 5-Bromoindole-2-carboxylic acid,Reactant involved in studies of biologically active molecules including:Discovery of indole inhibitors of MMP-13 for treatment of arthritic diseases1;Synthesis of indolyl ethanones as indoleamine 2,3-dioxygenase inhibitors2 ;cis-Diaminocyclohexane derivatives prepared for use as factor Xa inhibitors3 ;Synthesis of tubulin polymerization inhibitors and cancer cell growth inhibitors4 ;Preparation of dual PPARγ/δ agonists5;Synthesis of chemical probes to examine the role of hFPRL1 receptor . |
| | 5-Bromoindole-2-carboxylic acid Preparation Products And Raw materials |
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