2675-81-2 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
The compound is derived from benzene, a hydrocarbon with a six-carbon ring structure.
Explanation
These functional groups are attached to the benzene ring, giving the compound its unique properties and reactivity.
Explanation
The bromine atom is attached to the first carbon of the benzene ring.
Explanation
The chlorine atom is attached to the fourth carbon of the benzene ring.
Explanation
The two methoxy groups are attached to the second and fifth carbons of the benzene ring.
Explanation
The compound serves as a starting material for the production of other organic compounds, particularly in the pharmaceutical and chemical sectors.
Explanation
The compound can be used to create more complex molecular structures in organic synthesis.
Explanation
The presence of bromine and chlorine atoms allows for the development of various chemical structures, which can be useful in the creation of new drugs and materials.
Explanation
The methoxy groups contribute to the compound's reactivity and versatility in chemical reactions.
Explanation
Due to its chemical nature, it is important to handle the compound with care to avoid potential hazards.
Explanation
Proper safety measures should be taken when working with 1-bromo-4-chloro-2,5-dimethoxy-benzene to minimize the risk of exposure or accidents.
Derivative of benzene
Yes
Attached groups
Bromine, chlorine, and two methoxy (CH3O) groups
Position of bromine
1
Position of chlorine
4
Position of methoxy groups
2 and 5
Use in pharmaceutical and chemical industries
Precursor in the synthesis of various organic compounds
Use in organic synthesis
Building block for more complex molecules
Utility in drug development
Creation of diverse chemical structures
Reactivity and versatility
Influenced by methoxy groups
Hazardous properties
Potential hazards
Safety precautions
Handle with care
Check Digit Verification of cas no
The CAS Registry Mumber 2675-81-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,7 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2675-81:
(6*2)+(5*6)+(4*7)+(3*5)+(2*8)+(1*1)=102
102 % 10 = 2
So 2675-81-2 is a valid CAS Registry Number.
2675-81-2Relevant academic research and scientific papers
5-[3-[PIPERAZIN-1-YL]-3-OXO-PROPYL]-IMIDAZOLIDINE-2,4-DIONE DERIVATIVES AS ADAMTS 4 AND 5 INHIBITORS FOR TREATING E.G. OSTEOARTHRITIS
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Paragraph 0281, (2018/01/15)
The present invention discloses 5-[3-[piperazin-l-yl]-3-oxo-propyl]-imidazolidine-2,4-dione derivatives according to Formula (I), wherein R1, R2, R3a, R3b, R6a, R6b, the subscript n and Cy are as defined herein. The present invention relates to compounds inhibiting ADAMTS 4 and 5 for the prophylaxis or treatment of inflammatory diseases or diseases involving degradation of cartilage or disruption of cartilage homeostasis, such as e.g. osteoarthritis.
Accelerating Ni(ii) precatalyst initiation using reactive ligands and its impact on chain-growth polymerizations
Lee, Se Ryeon,Bloom, Jacob W. G.,Wheeler, Steven E.,McNeil, Anne J.
supporting information, p. 4218 - 4222 (2013/04/10)
Nickel(ii) complexes with varying reactive ligands, which were designed to selectively accelerate the initiation rate without influencing the propagation rate in the chain-growth polymerization of π-conjugated monomers, were investigated. Precatalysts with electronically varied reacting groups led to faster initiation rates and narrower molecular weight distributions. Computational studies revealed that the reductive elimination rates are largely modulated by the ability of the two reacting arenes to stabilize the increasing electron density on the catalyst during reductive elimination. Overall, these studies provide insight into a key mechanistic step of cross-coupling reactions (reductive elimination) and highlight the importance of initiation in controlled chain-growth polymerizations.
Chlorination increases the persistence of semiquinone free radicals derived from polychlorinated biphenyl hydroquinones and quinones
Song, Yang,Buettner, Garry R.,Parkin, Sean,Wagner, Brett A.,Robertson, Larry W.,Lehmler, Hans-Joachim
experimental part, p. 8296 - 8304 (2009/04/11)
(Chemical Equation Presented) Polychlorinated biphenyls (PCBs) comprise a group of persistent organic pollutants that differ significantly in their physicochemical properties, their persistence, and their biological activities. They can be metabolized via
