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5-(4-Chloroquinazolin-6-yl)furan-2-carbaldehyde is a chemical compound with the molecular formula C13H7ClN2O2. It is a derivative of quinazoline and furan, containing a furan-2-carbaldehyde moiety attached to a 4-chloroquinazolin-6-yl group. 5-(4-Chloroquinazolin-6-yl)furan-2-carbaldehyde has potential applications in medicinal chemistry and drug development, as it may exhibit various biological activities and pharmacological properties.

1334953-76-2

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1334953-76-2 Usage

Uses

Used in Pharmaceutical Industry:
5-(4-Chloroquinazolin-6-yl)furan-2-carbaldehyde is used as a potential pharmaceutical candidate for drug development due to its unique chemical structure and potential biological activities. Its synthesis and characterization are being researched to explore its potential uses in the development of new medications.
Used in Medicinal Chemistry Research:
5-(4-Chloroquinazolin-6-yl)furan-2-carbaldehyde is used as a subject of study in medicinal chemistry to understand its pharmacological properties and potential interactions with biological targets. This research can contribute to the discovery of new therapeutic agents and the advancement of drug design strategies.
It is important to handle 5-(4-Chloroquinazolin-6-yl)furan-2-carbaldehyde with care and follow proper safety protocols due to its chemical properties and potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 1334953-76-2 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 1334953-76:
(9*1)+(8*3)+(7*3)+(6*4)+(5*9)+(4*5)+(3*3)+(2*7)+(1*6)=172
172 % 10 = 2
So 1334953-76-2 is a valid CAS Registry Number.

1334953-76-2Downstream Products

1334953-76-2Relevant academic research and scientific papers

PROCESS AND INTERMEDIATES FOR PREPARING LAPATINIB

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Page/Page column 20-21, (2011/10/13)

Provided are a process for preparing lapatinib and its pharmaceutically acceptable salt by use of new intermediates, and a process for obtaining a pharmaceutical form of lapatinib ditosylate monohydrate.

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