530145-57-4 Usage
Chemical structure
A benzene ring with a bromine atom at the 1st position, three fluorine atoms at the 2nd, 3rd, and 4th positions, and an iodine atom at the 5th position.
Reactivity
Highly reactive due to the presence of strong electron-withdrawing groups (bromine, fluorine, and iodine atoms).
Versatility
Valuable building block for the synthesis of various biologically active molecules.
Applications
Used in organic synthesis, pharmaceutical research, and the production of pharmaceuticals, agrochemicals, and materials science.
Functional groups
Halogenated aromatic compound with bromine, fluorine, and iodine atoms.
Physical state
Likely a solid at room temperature, although specific information on its physical state is not provided in the material.
Stability
May be sensitive to heat, light, or moisture due to its high reactivity, but specific stability information is not provided in the material.
Hazards
Potential hazards are not mentioned in the material, but due to its reactivity, it may pose risks in certain conditions or upon contact with incompatible substances.
Purity
The material does not provide information on the purity of 1-bromo-2,3,4-trifluoro-5-iodobenzene, but it is generally expected to be synthesized and used in a pure form for specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 530145-57-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,0,1,4 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 530145-57:
(8*5)+(7*3)+(6*0)+(5*1)+(4*4)+(3*5)+(2*5)+(1*7)=114
114 % 10 = 4
So 530145-57-4 is a valid CAS Registry Number.
530145-57-4Relevant articles and documents
Organometallic control over the regiospecificity of functionalization reactions: 1,2,3-Trifluorobenzene and bromo derivatives thereof as substrates
Heiss, Christophe,Schlosser, Manfred
, p. 447 - 451 (2007/10/03)
In a case study, 1,2,3-trifluorobenzene was functionalized at each of the two vacant positions (producing the benzoic acids 1 and 2) and, in addition, bromine was introduced into all available positions (producing the benzoic acids 3-5). The required regioflexibility was achieved by applying novel organometallic recipes such as deprotonation-triggered halogen migrations and site-discriminating competitive halogen-metal permutations. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.
