315-65-1 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
The compound has a yellow color and a crystalline structure, which means it has a well-ordered arrangement of atoms.
Explanation
1,4-Naphthalenedione, 2-fluoroserves as a building block for creating more complex molecules, making it valuable in organic chemistry.
Explanation
The compound has been studied for its possible uses in various fields, including the development of new drugs and materials with specific properties.
Explanation
Due to its unique properties, 1,4-Naphthalenedione, 2-fluorocan be used in a wide range of chemical reactions, making it a versatile and useful compound in research.
Explanation
The potentially harmful nature of the compound requires that it be used carefully and in accordance with established safety protocols to minimize risks to human health and the environment.
Appearance
Yellow crystalline solid
Precursor in synthesis
Used as a starting material for the synthesis of other chemical compounds
Potential applications
Medicine and materials science
Versatile building block
Valuable tool for researchers and scientists
Safety precautions
Handle with caution and follow safety guidelines
Check Digit Verification of cas no
The CAS Registry Mumber 315-65-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,1 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 315-65:
(5*3)+(4*1)+(3*5)+(2*6)+(1*5)=51
51 % 10 = 1
So 315-65-1 is a valid CAS Registry Number.
315-65-1Relevant academic research and scientific papers
Synthesis of Fluoronaphthoquinones: Halide Displacement by Naked Fluoride
Cameron, Donald W.,Feutrill, Geoffrey I.,Griffiths, Peter G.,Richards, Kenneth R.
, p. 1509 - 1513 (2007/10/02)
Nucleophilic displacement of chloride or bromide from 2-halo-1,4-naphthoquinones has afforded easy synthesis of 2-fluoronaphthoquinones.The procedure involved mild treatment with unsolvated fluoride generated by crown polyether complexation of potassium fluoride in acetonitrile.
