363598-34-9 Usage
Aromatic compound
Contains a benzene ring with delocalized π electrons.
Halogenated compound
Contains two bromine (Br), two chlorine (Cl), and one fluorine (F) atoms.
Position of halogen atoms
Bromine atoms are at the 1st and 5th positions, chlorine atoms are at the 2nd and 4th positions, and the fluorine atom is at the 3rd position on the benzene ring.
Applications
a. Intermediate in the synthesis of pharmaceuticals and agrochemicals.
b. Building block in the production of dyes, polymers, and other organic compounds.
Reactivity
Highly reactive due to the presence of multiple halogens.
Versatility
Utilized in various industrial and scientific applications.
Physical state
Likely a solid at room temperature, based on its molecular weight and structure.
Stability
May be sensitive to heat, light, or moisture due to the presence of multiple halogens.
Hazards
Potentially toxic and harmful if inhaled, ingested, or absorbed through the skin. Proper handling and storage are necessary to minimize risks.
Check Digit Verification of cas no
The CAS Registry Mumber 363598-34-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,3,5,9 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 363598-34:
(8*3)+(7*6)+(6*3)+(5*5)+(4*9)+(3*8)+(2*3)+(1*4)=179
179 % 10 = 9
So 363598-34-9 is a valid CAS Registry Number.
363598-34-9Relevant articles and documents
Extensive halogen scrambling and buttressing effects encountered upon treatment of oligobromoarenes with bases
Mongin, Florence,Marzi, Elena,Schlosser, Manfred
, p. 2771 - 2777 (2007/10/03)
As a rule, tri-, tetra- and pentahaloarenes readily undergo ortho-lithiation when treated with amide-type bases. However, halogen migration occurs whenever the substrate contains three or more contiguous halogen atoms, provided that at least one of them is bromine or iodine. Dismutation and reduction processes often take place concomitantly. In this manner, a variety of organometallic intermediates may be formed, the driving force always being a decrease in basicity. When no such energy gain can be achieved, a sterically crowded substrate may just turn out to be inert; this was found to be the case with 1,5-dibromo-3-fluoro-2-(trimethylsilyl)benzene, 1,5-dibromo-3-fluoro-2,4-bis(trimethylsilyl)benzene, and 1,5-dibromo-3-fluoro-2,4-diiodobenzene. Buttressing effects are apparently strong enough to prevent expedient deprotonation of those substrates.
