cas 149353-75-3|| where to buy 4-(1-(tert-Butoxycarbonyl)piperidin-4-yl)benzoic acid

Produktname:4-(1-(tert-Butoxycarbonyl)piperidin-4-yl)benzoic acid

IUPAC Name:4-{1-[(tert-butoxy)carbonyl]piperidin-4-yl}benzoic acid

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CM160278-5g	in stock	ưưǕ
CM160278-10g	in stock	ŢƄƄ
CM160278-25g	in stock	ƞȀƞ
CM160278-100g	in stock	ŢŢȎȀ

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: CAS-Nr.:149353-75-3; Molekulare Formel:C17H23NO4; Schmelzpunkt:-; SMILES-Code:CC(C)(C)OC(=O)N1CCC(CC1)C1=CC=C(C=C1)C(O)=O; Dichte:

: Katalognummer:CM160278; Molekulargewicht:305.37; Siedepunkt:448°C at 760 mmHg; Mdl-Nr.:MFCD02178897; Lagerung:Store at 2-8°C.

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: 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.

: Tasurgratinib; Eisai announced that it has obtained manufacturing and marketing approval for fibroblast growth factor receptor (FGFR) selective tyrosine kinase inhibitor ‘TASFYGO® Tablets 35mg’ (tasurgratinib succinate) in Japan for the treatment of patients with unresectable biliary tract cancer with FGFR2 gene fusions or rearrangements that progressed after cancer chemotherapy. In Japan, it has received orphan drug designation from the Ministry of Health, Labour and Welfare (MHLW), and the marketing authorization application was submitted in December 2023. TASFYGO is an orally available novel tyrosine kinase inhibitor that demonstrates selective inhibitory activity against fibroblast growth factor receptors (FGFR) FGFR1, FGFR2 and FGFR3.
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