| Identification | |
| Name: | 5-Bromoindole-2-carboxylic acid |
| Synonyms: | 5-bromo-1H-indole-2-carboxylic acid; |
| CAS: | 7254-19-5 |
| Molecular Formula: | C9H6BrNO2 |
| Molecular Weight: | 240.05 |
| InChI: | InChI=1/C9H6BrNO2/c10-6-1-2-7-5(3-6)4-8(11-7)9(12)13/h1-4,11H,(H,12,13) |
| Molecular Structure: |  |
| Properties | |
| Melting Point: | 287-288 |
| Flash Point: | 238.611°C |
| Boiling Point: | 470.932°C at 760 mmHg |
| Density: | 1.838g/cm3 |
| Refractive index: | 1.749 |
| Specification: | usageEng: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 in inflammation6 Safety Statements:26-37/39 26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice 37/39:Wear suitable protective clothing, gloves and eye/face protection |
| HS Code: | 29339980 |
| Flash Point: | 238.611°C |
| Usage: | 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 in inflammation6 |
| Safety Data | |
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