cas 5013-77-4|| where to buy 1-(2,4-Dichlorophenyl)-N-methylmethanamine

Nom du produit:1-(2,4-Dichlorophenyl)-N-methylmethanamine

IUPAC Name:[(2,4-dichlorophenyl)methyl](methyl)amine

Unité d'emballage	Stock disponible	Prix($)
CM108091-25g	in stock	ƴƐ
CM108091-100g	in stock	œƚŸ
CM108091-500g	in stock	ƐȅŸ

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: N° CAS:5013-77-4; Formule moléculaire:C8H9Cl2N; Point de fusion:-; Code SMILES:CNCC1=CC=C(Cl)C=C1Cl; Densité:

: Numéro de catalogue:CM108091; Poids moléculaire:190.07; Point d'ébullition:240.6°C at 760 mmHg; N° Mdl:MFCD00045185; Stockage:Keep in dark place, store at 2-8°C.

: 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.

: Nitrogen Compounds; Nitrogen compounds can be classified as mineral or organic. Mineral compounds are essentially formed by the ammonium ion (NH4+), which is generated when ammonium salts are dissolved in water. Organic compounds, in contrast, are carbon and hydrogen compounds that contain a nitrogen atom. All organic nitrogen-containing compounds can be considered as derivatives of ammonia in which one or more hydrogen atoms are substituted by hydrocarbon radicals.

: Tenapanor; FDA has approved XPHOZAH (tenapanor), the first and only phosphate absorption inhibitor, indicated to reduce serum phosphorus in adults with chronic kidney disease (CKD) on dialysis as add-on therapy in patients who have an inadequate response to phosphate binders or who are intolerant of any dose of phosphate binder therapy.

XPHOZAH, with its unique blocking mechanism of action, acts locally in the gut to inhibit the sodium hydrogen exchanger 3 (NHE3), reducing phosphate absorption through the paracellular pathway, the primary pathway of phosphate absorption.