366496-32-4 Usage
Description
2,4,5-Tribromoiodobenzene is an organic compound that serves as an intermediate in the synthesis of various chemicals. It is characterized by its unique structure, which includes three bromine atoms and one iodine atom attached to a benzene ring.
Uses
Used in Chemical Synthesis:
2,4,5-Tribromoiodobenzene is used as an intermediate in the synthesis of 2,2'',4,4'',5,6''-Hexabromodiphenyl ether (H290745), a hepatotoxic polybrominated diphenyl ester (PBDE) commonly utilized as a flame retardant. Its role in the production process is crucial for creating this compound with desired properties.
Used in Flame Retardants Industry:
2,4,5-Tribromoiodobenzene is used as a precursor for the production of 2,2'',4,4'',5,6''-Hexabromodiphenyl ether, which is an essential component in the flame retardants industry. This application is significant due to the increasing demand for materials that can reduce the risk of fire in various products, such as electronics and textiles.
Used in Environmental and Health Risk Assessment:
2,4,5-Tribromoiodobenzene, through its derivative 2,2'',4,4'',5,6''-Hexabromodiphenyl ether, is sometimes found in food and meats, posing a significant risk to humans and animals that consume it. As a result, it is used in environmental and health risk assessment to evaluate the potential hazards associated with the presence of these compounds in the food chain, particularly during pregnancy.
Used in the Stockholm Convention:
2,4,5-Tribromoiodobenzene's derivative, 2,2'',4,4'',5,6''-Hexabromodiphenyl ether, is one of the new Persistent Organic Pollutants (POPs) under the Stockholm Convention. This international treaty aims to protect human health and the environment from the harmful effects of these chemicals. 2,4,5-tribromoiodobenzene's role in this context is to raise awareness and promote the development of safer alternatives to reduce the environmental and health risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 366496-32-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,6,4,9 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 366496-32:
(8*3)+(7*6)+(6*6)+(5*4)+(4*9)+(3*6)+(2*3)+(1*2)=184
184 % 10 = 4
So 366496-32-4 is a valid CAS Registry Number.
366496-32-4Relevant articles and documents
Conformational regulation of multivalent terpyridine ligands for self-assembly of heteroleptic metallo-supramolecules
Wang, Shi-Cheng,Cheng, Kai-Yu,Fu, Jun-Hao,Cheng, Yuan-Chung,Chan, Yi-Tsu
, p. 16661 - 16667 (2020)
A two-ligand system composed of the predesigned multivalent and complementary terpyridine-based ligands was exploited to construct heteroleptic metallo-supramolecules and to investigate the self-assembly mechanism. Molecular stellation of the trimeric hex
Synthesis of bent [4]phenylene (cyclobuta[1,2-a:3,4-b′]bisbiphenylene) and structure of a bis(trimethylsilyl) derivative: The last [4]phenylene isomer
Bong, Dennis T.-Y.,Gentric, Lionel,Holmes, Daniel,Matzger, Adam J.,Scherhag, Frank,Vollhardt
, p. 278 - 279 (2007/10/03)
The syntheses of the title compounds were accomplished by cobalt-catalyzed alkyne cyclotrimerizations using two strategies; the properties of the bent phenylene frame reflect the combined effects of benzocyclobutadienofusion of the component [3]phenylene
