cas 1075705-01-9|| where to buy 4-Fluoro-2-methoxy-5-nitroaniline

Название продукции:4-Fluoro-2-methoxy-5-nitroaniline

IUPAC Name:4-fluoro-2-methoxy-5-nitroaniline

: CAS：1075705-01-9; Молекулярная формула：C7H7FN2O3; Чистота：95%+

Упаковочная единица	Доступно для заказа	Цена ($)
CM118763-500g	in stock	ĳŌħ
CM118763-1000g	in stock	Ǹǎħ

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: Номер CAS:1075705-01-9; Молекулярная формула:C7H7FN2O3; Точка плавления:-; Smiles-код:NC1=CC([N+]([O-])=O)=C(F)C=C1OC; Плотность:

: Номер в каталоге:CM118763; Молекулярная масса:186.14; Точка кипения:; Номер Mdl:MFCD23098941; Хранение:

: 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.

: Lazertinib; Johnson & Johnson announced new data from the Phase 2 PALOMA-2 study evaluating subcutaneous (SC) amivantamab combined with lazertinib as a first-line treatment in patients with advanced non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 19 deletion or L858R mutations. These data showed a comparable response rate in patients treated with SC amivantamab and lazertinib compared to those treated with the intravenous (IV) formulation in the MARIPOSA study, which established the combination of amivantamab and lazertinib as superior to osimertinib. Lazertinib is an oral, third-generation, brain-penetrant EGFR tyrosine kinase inhibitor (TKI) that targets both the T790M mutation and activating EGFR mutations while sparing wild type-EGFR.
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