4,7-Dimethyl-1H-indazole-3-carbaldehyde
CAS No.:
1000340-75-9
M. Wt:
174.199
M. Fa:
C10H10N2O
InChI Key:
AXNSIRJXHHTZIQ-UHFFFAOYSA-N
Names and Identifiers of 4,7-Dimethyl-1H-indazole-3-carbaldehyde
CAS Number |
1000340-75-9 |
|---|---|
MDL Number |
MFCD28162985 |
IUPAC Name |
4,7-dimethyl-2H-indazole-3-carbaldehyde |
InChI |
InChI=1S/C10H10N2O/c1-6-3-4-7(2)10-9(6)8(5-13)11-12-10/h3-5H,1-2H3,(H,11,12) |
InChIKey |
AXNSIRJXHHTZIQ-UHFFFAOYSA-N |
Canonical SMILES |
CC1=CC=C(C2=NNC(=C12)C=O)C |
UNSPSC Code |
12352100 |
Physical and chemical properties of 4,7-Dimethyl-1H-indazole-3-carbaldehyde
Boiling Point |
374.7±37.0 °C at 760 mmHg |
|---|---|
Density |
1.3±0.1 g/cm3 |
Exact Mass |
174.079315 |
Flash Point |
183.8±32.9 °C |
H Bond Acceptors |
2 |
H Bond Donors |
1 |
Index of Refraction |
1.686 |
LogP |
1.96 |
Molecular Formula |
C10H10N2O |
Molecular Weight |
174.199 |
PSA |
45.75000 |
Vapour Pressure |
0.0±0.8 mmHg at 25°C |
Safety Information of 4,7-Dimethyl-1H-indazole-3-carbaldehyde
Applications of 4,7-Dimethyl-1H-indazole-3-carbaldehyde
4,7-Dimethyl-1H-indazole-3-carbaldehyde has several potential applications:
- Pharmaceutical Development: Its derivatives may serve as lead compounds in drug discovery due to their biological activities.
- Organic Synthesis: It is useful as an intermediate in synthesizing other complex organic molecules.
- Material Science: Its unique structure may find applications in developing novel materials or catalysts.
Biological Activity of 4,7-Dimethyl-1H-indazole-3-carbaldehyde
Research indicates that compounds related to 4,7-dimethyl-1H-indazole-3-carbaldehyde exhibit various biological activities. Indazole derivatives have been studied for their potential anti-inflammatory, anticancer, and antimicrobial properties. For instance, some indazole derivatives act as inhibitors of certain kinases involved in cancer progression, suggesting that this compound may also possess similar bioactivity.
