844879-16-9 Usage
Uses
Used in Pharmaceutical Research:
(4-Bromophenyl)-(3,5-dimethylphenyl)-methanone is used as a building block in the production of various pharmaceutical drugs and active pharmaceutical ingredients (APIs). Its structural properties make it a valuable component in the development of new medications.
Used in Organic Synthesis:
(4-Bromophenyl)-(3,5-dimethylphenyl)-methanone serves as an intermediate in the synthesis of various biologically active compounds, contributing to the creation of a wide range of chemical products with potential applications in different industries.
Used as a Reagent:
(4-Bromophenyl)-(3,5-dimethylphenyl)-methanone can be utilized as a reagent in organic chemical reactions, facilitating the formation of new compounds and contributing to the advancement of chemical research.
Used in Medicinal Chemistry and Drug Discovery:
Due to its pharmacological properties, (4-Bromophenyl)-(3,5-dimethylphenyl)-methanone may have potential applications in the field of medicinal chemistry and drug discovery, where it could be instrumental in the development of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 844879-16-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,4,8,7 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 844879-16:
(8*8)+(7*4)+(6*4)+(5*8)+(4*7)+(3*9)+(2*1)+(1*6)=219
219 % 10 = 9
So 844879-16-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H13BrO/c1-10-7-11(2)9-13(8-10)15(17)12-3-5-14(16)6-4-12/h3-9H,1-2H3
844879-16-9Relevant academic research and scientific papers
Preparation of functionalized organoaluminiums by direct insertion of aluminium to unsaturated halides
Blumke, Tobias,Chen, Yi-Hung,Peng, Zhihua,Knochel, Paul
supporting information; experimental part, p. 313 - 318 (2010/09/05)
The preparation of polyfunctional organometallics is important in organic synthesis as these reagents are very popular nucleophiles. The preparation of functionalized aluminium reagents by direct insertion of aluminium powder is in general not possible. Such a reaction would be of special importance owing to the low price of aluminium compared with magnesium (it is half the price), the low toxicity of this metal and the chemoselectivity of the resultant organoaluminium reagents. We have now found that by adding catalytic amounts of selected metallic chlorides (TiCl4, BiCl3, InCl 3 or PbCl2) in the presence of LiCl, aluminium powder inserts into various unsaturated iodides and bromides under mild conditions. These resulting new organoaluminium reagents undergo smooth Pd-catalysed cross-coupling and acylation reactions, as well as copper-catalysed allylic substitutions, affording various interesting products for pharmaceutical and material science applications.
