cas 403-16-7|| where to buy 3-Chloro-4-fluorobenzoic acid

Nom du produit:3-Chloro-4-fluorobenzoic acid

IUPAC Name:3-chloro-4-fluorobenzoic acid

Unité d'emballage	Stock disponible	Prix($)
CM157718-100g	in stock	ŮŤ
CM157718-500g	in stock	ǸƴŮ

Pour une utilisation en R&D uniquement..

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: N° CAS:403-16-7; Formule moléculaire:C7H4ClFO2; Point de fusion:-; Code SMILES:O=C(O)C1=CC=C(F)C(Cl)=C1; Densité:

: Numéro de catalogue:CM157718; Poids moléculaire:174.56; Point d'ébullition:287.4°C at 760 mmHg; N° Mdl:MFCD00042477; Stockage:Store at room temperature.

: 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.

: LEI-515; The recent publication titles “Structure–Activity Relationship Studies of Aryl Sulfoxides as Reversible Monoacylglycerol Lipase Inhibitors”. Monoacylglycerol lipase (MAGL) is the critical enzyme responsible for the hydrolysis of endocannabinoid 2-arachidonoylglycerol (2-AG) to arachidonate and glycerol, contributing to the inflammatory cascade in the CNS. MAGL inhibition provides various potential therapeutic opportunities, including inflammation-induced tissue injury, pain, multiple sclerosis, and cancer.
LEI-515 is an aryl sulfoxide, and a peripherally restricted, covalent reversible MAGL inhibitor. LEI-515 increases 2-AG levels in the periphery and reduces neuropathic pain and inflammation, without inducing CNS adverse effects or physical dependence.