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Pyrroles

Aromatic organic heterocyclic compounds that consist of a five-membered ring with four carbon atoms and one nitrogen atom that forms an amine functional group.
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1

5-(2-Fluorophenyl)pyrrole-3-carboxaldehyde 98.0+%, TCI America™

CAS: 881674-56-2 Molecular Formula: C11H8FNO Molecular Weight (g/mol): 189.19 MDL Number: MFCD11875867 InChI Key: MQULPEUCGKEHEG-UHFFFAOYSA-N PubChem CID: 46908593 IUPAC Name: 5-(2-fluorophenyl)-1H-pyrrole-3-carbaldehyde SMILES: FC1=CC=CC=C1C1=CC(C=O)=CN1

PubChem CID 46908593
CAS 881674-56-2
Molecular Weight (g/mol) 189.19
MDL Number MFCD11875867
SMILES FC1=CC=CC=C1C1=CC(C=O)=CN1
IUPAC Name 5-(2-fluorophenyl)-1H-pyrrole-3-carbaldehyde
InChI Key MQULPEUCGKEHEG-UHFFFAOYSA-N
Molecular Formula C11H8FNO
2

eMolecules​ 4-Bromo-2-chloro-3-fluoropyridine | 1211526-56-5 | MFCD16606306 | 1g

Ambeed | 4-Bromo-2-chloro-3-fluoropyridine | 1g | 525017445 | A119702 | | 1211526-56-5 | MFCD16606306 | 210.430 | C5H2BrClFN

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3

Medchemexpress LLC Pha-665752 | 477575-56-7 | MFCD18632554; MFCD07772270 | 99.9% | 641.61 g/mol | C32H34Cl2N4O4S | 5 MG
SDP

PHA-665752 is a selective, ATP-competitive inhibitor of the c-Met (HGFR) receptor tyrosine kinase used in preclinical research to induce apoptosis, cause cell-cycle arrest, and reduce tumor growth in vitro and in vivo. It demonstrates high potency and selectivity versus other kinases and is supplied for research use only.

  • Selective ATP-competitive c-Met inhibitor with Ki ≈ 4 nM and IC50 ≈ 9 nM.
  • High purity solid (approximately 99.9%) suitable for biochemical assays.
  • Molecular formula C32H34Cl2N4O4S; molecular weight 641.61 g/mol.
  • Storage: powder at -20°C for long term; in solution store at -80°C when possible.
  • Supplied in small preweighed milligram quantities for laboratory research.

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