1334953-74-0 Usage
Description
6-(5-((2-(Methylsulfonyl)ethylaMino)Methyl)furan-2-yl)quinazolin-4(3h)-one is a complex chemical compound with a quinazolin-4(3h)-one core, featuring a furan-2-yl substituent and a 2-(Methylsulfonyl)ethylaminoethyl substituent. Its molecular structure suggests potential pharmacological properties, given the presence of the quinazolin-4(3h)-one core, which is a common element in many drugs and biologically active molecules.
Uses
Used in Pharmaceutical Industry:
6-(5-((2-(Methylsulfonyl)ethylaMino)Methyl)furan-2-yl)quinazolin-4(3h)-one is used as a potential pharmaceutical agent for its possible pharmacological activity. The presence of the quinazolin-4(3h)-one core and the additional substituents may contribute to its potential therapeutic applications, although further research is required to fully understand its properties and efficacy.
Used in Drug Development Research:
In the field of drug development, 6-(5-((2-(Methylsulfonyl)ethylaMino)Methyl)furan-2-yl)quinazolin-4(3h)-one serves as a candidate molecule for investigation into its pharmacological properties. Its unique structure may offer insights into the development of new drugs and therapies, pending further exploration and validation through scientific studies.
Check Digit Verification of cas no
The CAS Registry Mumber 1334953-74-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,4,9,5 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1334953-74:
(9*1)+(8*3)+(7*3)+(6*4)+(5*9)+(4*5)+(3*3)+(2*7)+(1*4)=170
170 % 10 = 0
So 1334953-74-0 is a valid CAS Registry Number.
1334953-74-0Relevant articles and documents
EFFICIENT PROCESS FOR THE PREPARATION OF LAPATINIB AND SALTS THEREOF BY MEANS OF NEW INTERMEDIATES
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, (2015/03/16)
The present invention refers to a new efficient process for the synthesis of the active pharmaceutical ingredient Lapatinib and salts thereof. In particular, the present synthesis is carried out employing new intermediates in which the amine function is protected by a group cleavable in basic milieu that provides a higher overall yield of the synthesis process.
Efficient process for the preparation of Lapatinib and salts thereof by means of new intermediates
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, (2014/07/23)
The present invention refers to a new efficient process for the synthesis of the active pharmaceutical ingredient Lapatinib and salts thereof. In particular, the present synthesis is carried out employing new intermediates in which the amine function is protected by a group cleavable in basic milieu that provides a higher overall yield of the synthesis process.
Process for the preparation of lapatinib and the salts thereof
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, (2012/07/03)
The present invention refers to a new process for the synthesis of the pharmaceutical active ingredient Lapatinib and the salts thereof. In particular, the present synthesis is performed using intermediates in which the hydroxyl function is protected by the tetrahydropyranyl group hence entailing greater solubility of the intermediates in the common organic solvents.
