679836-60-3 Usage
Structure
A derivative of benzene with two bromine atoms, two fluorine atoms, and one iodine atom attached to its carbon ring.
Functional groups
Bromine (Br), Fluorine (F), and Iodine (I) atoms.
Appearance
Unknown, but likely a solid or liquid depending on temperature.
Physical state
Unknown, but likely solid or liquid at room temperature.
Polarity
Likely polar due to the presence of multiple electronegative atoms (Br, F, and I).
Solubility
Likely soluble in organic solvents such as dichloromethane, acetone, or ethyl acetate.
Boiling point
Unknown, but expected to be relatively high due to the presence of heavy atoms (Br, F, and I).
Melting point
Unknown, but expected to be relatively low due to the presence of multiple halogen atoms.
Density
Unknown, but likely higher than water due to the presence of heavy atoms (Br, F, and I).
Reactivity
Likely reactive with nucleophiles and electrophiles due to the presence of electronegative atoms (Br, F, and I).
Uses
Commonly used as a building block in organic synthesis and pharmaceutical research.
Applications
Versatile intermediate in the creation of various pharmaceuticals and agrochemicals.
Importance
Important tool in the development of new drug candidates and other biologically active molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 679836-60-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,9,8,3 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 679836-60:
(8*6)+(7*7)+(6*9)+(5*8)+(4*3)+(3*6)+(2*6)+(1*0)=233
233 % 10 = 3
So 679836-60-3 is a valid CAS Registry Number.
679836-60-3Relevant academic research and scientific papers
Synthesis and thiolation of 1,3-difluoro-2,4,6-trihaloanilines and benzenes
Manka, Jason T.,Kaszynski, Piotr
, p. 39 - 43 (2007/10/03)
Three pentahaloanilines were prepared by stepwise halogenation of 3,5-difluoroaniline and were deaminated to form pentahalobenzenes. Alternatively, two pentahalobenzenes were obtained by lithiation followed by iodination of 1,3-difluoro-4,6-dihalobenzenes
