Nom du produit:4-formyl-3-methoxybenzonitrile
IUPAC Name:4-formyl-3-methoxybenzonitrile
- CAS:21962-45-8
- Formule moléculaire:C9H7NO2
- Pureté:98%
- Numéro de catalogue:CM156985
- Poids moléculaire:161.16
Pour une utilisation en R&D uniquement..
Détails du produit
- N° CAS:21962-45-8
- Formule moléculaire:C9H7NO2
- Point de fusion:-
- Code SMILES:N#CC1=CC=C(C=O)C(OC)=C1
- Densité:
- Numéro de catalogue:CM156985
- Poids moléculaire:161.16
- Point d'ébullition:318.2°C at 760 mmHg
- N° Mdl:MFCD07779491
- Stockage:Keep in a tight container and store at 2°C~8°C
Category Infos
- Benzenes
- Benzene is an important organic compound with the chemical formula C6H6, and its molecule consists of a ring of 6 carbon atoms, each with 1 hydrogen atom. Benzene is a sweet, flammable, colorless and transparent liquid with carcinogenic toxicity at room temperature, and has a strong aromatic odor. It is insoluble in water, easily soluble in organic solvents, and can also be used as an organic solvent itself. The ring system of benzene is called benzene ring, and the structure after removing one hydrogen atom from the benzene ring is called phenyl. Benzene is one of the most important basic organic chemical raw materials. Many important chemical intermediates can be derived from benzene through substitution reaction, addition reaction and benzene ring cleavage reaction.
Column Infos
- Finerenone
- Bayer announced that FINEARTS-HF met its primary endpoint, achieving a statistically significant reduction of the composite of cardiovascular death and total (first and recurrent) heart failure (HF) events, defined as hospitalizations for HF or urgent HF visits. The randomized, double-blind, placebo-controlled, parallel-group, multi-center phase III cardiovascular outcomes study evaluated the efficacy and safety of KERENDIA® (finerenone) for investigational new use in patients with HF with a LVEF≥40% (left ventricular ejection fraction). Finerenone is a nonsteroidal mineralocorticoid receptor antagonist (MRA) that was approved to reduce the risk of cardiovascular death, non-fatal myocardial infarction, hospitalization for heart failure, sustained eGFR decline, and end-stage kidney disease in adult patients with CKD associated with T2D.
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