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80761-61-1

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80761-61-1 Usage

Uses

1,4-Dihydro-4-oxo-3-quinolinecarbonyl Chloride is an intermediate in synthesizing Ivacaftor Carboxylic Acid (I940605). It is an impurity of Ivacaftor (I940600); a drug used in the treatment of cystic fibrosis.

Check Digit Verification of cas no

The CAS Registry Mumber 80761-61-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,7,6 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80761-61:
(7*8)+(6*0)+(5*7)+(4*6)+(3*1)+(2*6)+(1*1)=131
131 % 10 = 1
So 80761-61-1 is a valid CAS Registry Number.

80761-61-1Relevant articles and documents

Quinolone-based oxazolidinone compound as well as preparation method and application thereof

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Paragraph 0099-0101, (2021/07/31)

The invention discloses a quinolone-based oxazolidinone compound with a formula (HB), a solvate thereof, a stereoisomer of the compound, or a pharmaceutically acceptable salt of the compound, a preparation method of the compound and application of the com

Discovery of N -(2,4-Di- tert -butyl-5-hydroxyphenyl)-4-oxo-1,4-dihydroquinoline-3-carboxamide (VX-770, Ivacaftor), a potent and orally bioavailable CFTR potentiator

Hadida, Sabine,Van Goor, Fredrick,Zhou, Jinglan,Arumugam, Vijayalaksmi,McCartney, Jason,Hazlewood, Anna,Decker, Caroline,Negulescu, Paul,Grootenhuis, Peter D. J.

, p. 9776 - 9795 (2015/01/16)

Quinolinone-3-carboxamide 1, a novel CFTR potentiator, was discovered using high-throughput screening in NIH-3T3 cells expressing the F508del-CFTR mutation. Extensive medicinal chemistry and iterative structure-activity relationship (SAR) studies to evaluate potency, selectivity, and pharmacokinetic properties resulted in the identification of N-(2,4-di-tert-butyl-5-hydroxyphenyl)-4-oxo-1,4-dihydroquinoline-3-carboxamide (VX-770, 48, ivacaftor), an investigational drug candidate approved by the FDA for the treatment of CF patients 6 years of age and older carrying the G551D mutation.

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