1484038-03-0 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
This describes the arrangement of atoms and functional groups in the molecule, which determines its chemical properties and reactivity.
Explanation
These functional groups contribute to the compound's reactivity and its potential applications in various industries.
Explanation
The compound's properties make it useful in creating new compounds and products in various fields, including medicine and agriculture.
Explanation
Due to its unique properties and potential applications, the compound is considered important for the development and advancement of multiple sectors.
Explanation
The compound can be further modified or reacted with other molecules to create a wide range of products, making it a versatile building block in chemical synthesis.
Chemical structure
Chloro-substituted fluorobenzene derivative with a 2,4-dimethoxybenzyl group attached to the third carbon atom.
Functional groups
Chlorine (Cl), Fluorine (F), and two methoxy groups (-OCH3) on the benzyl group.
Applications
Organic synthesis, pharmaceutical research, production of pharmaceuticals and agrochemicals, development of new materials and technologies.
Industry relevance
Valuable for various industries and scientific research.
Building block
Used as a starting material for the synthesis of more complex molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 1484038-03-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,8,4,0,3 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1484038-03:
(9*1)+(8*4)+(7*8)+(6*4)+(5*0)+(4*3)+(3*8)+(2*0)+(1*3)=160
160 % 10 = 0
So 1484038-03-0 is a valid CAS Registry Number.
1484038-03-0Relevant articles and documents
PROCESS AND INTERMEDIATES FOR PREPARING INTEGRASE INHIBITORS
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, (2014/02/16)
The invention provides synthetic processes and synthetic intermediates that can be used to prepare 4-oxoquinolone compounds having useful integrase inhibiting properties.
