Nom du produit:ethyl 2,4-dimethyl-1H-pyrrole-3-carboxylate

IUPAC Name:ethyl 2,4-dimethyl-1H-pyrrole-3-carboxylate

CAS:2199-51-1
Formule moléculaire:C9H13NO2
Pureté:95%+
Numéro de catalogue:CM103853
Poids moléculaire:167.21

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Détails du produit

N° CAS:2199-51-1
Formule moléculaire:C9H13NO2
Point de fusion:-
Code SMILES:CCOC(=O)C1=C(C)NC=C1C
Densité:
Numéro de catalogue:CM103853
Poids moléculaire:167.21
Point d'ébullition:291°C at 760 mmHg
N° Mdl:MFCD01365811
Stockage:Store at room temperature

Category Infos

Pyrroles
Pyrrole is a five membered heterocyclic compound with the molecular formula of C4H5N. Pyrrole has a ring composed of four carbon atoms and one nitrogen atom. Pyrrole is easy to polymerize in the air. Pyrrole is the parent compound of many important biological substances (such as bile pigment, porphyrin and chlorophyll). Pyrrole scaffolds are widely used in biological and pharmaceutical fields. Pyrrole is a special heterocyclic scaffold, which exists in many natural products, drug molecules and pesticides, and has shown its application in materials science.
Pyrrole,Where to Buy Pyrroles-Chemenu
Pyrrole,Where to Buy Pyrroles
Pyrrole is a heterocyclic, aromatic, organic compound, a five-membered ring with the formula C 4H 4NH. It is a colorless volatile liquid that darkens readily upon exposure to air. Substituted derivatives are also called pyrroles, e.g., N-methylpyrrole.

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Vorolanib
EyePoint Pharmaceuticals announced on December 4th announced positive topline results of its Phase 2 DAVIO 2 trial of EYP-1901, an investigational sustained delivery maintenance treatment for wet age-related macular degeneration (wet AMD) combining vorolanib, a selective tyrosine kinase inhibitor with bioerodible Durasert E™. Vorolanib brings a new mechanistic approach to the treatment of VEGF-mediated retinal diseases as a pan-VEGF receptor blocker, blocking all VEGF isoforms. Vorolanib features reduced off-target binding and at clinically relevant doses does not inhibit Tie-2, a critical pathway associated with vascular stability, which may result in an improved efficacy. Further, in an in-vivo model of retinal detachment, vorolanib demonstrated neuroprotection, and potential antifibrotic benefits.