Oxidative activation of 2-methylindole-3-carboxaldehyde via N-heterocyclic carbene organocatalysis generates heterocyclic ortho-quinodimethane as a key intermediate.Reactant for preparation of: 1.Tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators. 2.Fluorescent sensors (BODIPY). 3.Antimicrobial agents against methicillin-resistant Staphylococcus aureus. 4.G protein-coupled receptor CRTh2 antagonists. 5.Inhibitors of PI3 kinase-α. 6.Antitubercular agents. 7.Anti-inflammatory agents. 8.Mycobacterium tuberculosis protein tyrosine phosphatase B. 9.Glucocorticoid receptor ligands. 10.Agents stimulating neurite outgrowth.
Specifications and Purity: ≥98%(GC)
MDL Number: MFCD00012077
Molecular Formula: C10H9NO
Molecular Weight: 159.18
EC Number: 226-512-6
PubChem CID: 73166
Isomeric SMILES: CC1=C(C2=CC=CC=C2N1)C=O
Beilstein Registry Number: 21(5)8,306
Related Documents: https://aladdin-for-icloud-store.oss-cn-hangzhou.aliyuncs.com/aladdinsci/pdp/sds/1/M123431-SCI_9912e912011037fcbafa4845680651c6.pdf
- UPC:
- 12352114
- Condition:
- New
- HazmatClass:
- No
- WeightUOM:
- LB
- MPN:
- M123431-25g
- CAS:
- 5416-80-8
- Product Size:
- 25g
- Hazard Statement Codes:
- H335:H319:H315:H302
- Precautionary Statement Codes:
- P501:P403+P233:P405:P362+P364:P305+P351+P338:P304+P340:P302+P352:P301+P312:P330:P280:P271:P270:P264:P261
akash.verma@cenmed.com
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