62606-15-9 Usage
Uses
Used in Organic Synthesis:
1-Bromo-3-methanesulfonyl-5-nitrobenzene is used as a reagent in organic synthesis for the introduction of the bromomethylsulfonyl group into various organic compounds. Its ability to facilitate the formation of new chemical bonds makes it a valuable tool in creating a wide range of chemical products.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 1-Bromo-3-methanesulfonyl-5-nitrobenzene serves as a precursor in the synthesis of various pharmaceuticals. Its unique chemical structure contributes to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Synthesis:
Similarly, in agrochemical synthesis, 1-Bromo-3-methanesulfonyl-5-nitrobenzene is utilized as a precursor to develop new compounds for agricultural use, such as pesticides and herbicides, to improve crop protection and yield.
Used in Medicinal Chemistry Research:
1-Bromo-3-methanesulfonyl-5-nitrobenzene is also used in medicinal chemistry research for its potential anti-cancer properties. Studies are being conducted to explore its ability to target and inhibit the growth of cancer cells, offering a promising avenue for the development of novel cancer treatments.
Used in Drug Development:
In the context of drug development, 1-Bromo-3-methanesulfonyl-5-nitrobenzene is recognized for its potential anti-inflammatory properties. Researchers are investigating its capacity to modulate inflammatory responses, which could lead to the creation of new anti-inflammatory medications.
Check Digit Verification of cas no
The CAS Registry Mumber 62606-15-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,0 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62606-15:
(7*6)+(6*2)+(5*6)+(4*0)+(3*6)+(2*1)+(1*5)=109
109 % 10 = 9
So 62606-15-9 is a valid CAS Registry Number.
62606-15-9Relevant academic research and scientific papers
Pd-Catalyzed Decarboxylative Ortho-Halogenation of Aryl Carboxylic Acids with Sodium Halide NaX Using Carboxyl as a Traceless Directing Group
Fu, Zhengjiang,Jiang, Yongqing,Wang, Shuiliang,Song, Yuanyuan,Guo, Shengmei,Cai, Hu
supporting information, p. 3003 - 3007 (2019/05/10)
A highly regioselective Pd-catalyzed carboxyl directed decarboxylative ortho-C-H halogenation of cheap o-nitrobenzoic acids with NaX (X = I, Br) under aerobic conditions has been established. The utility of the method has been demonstrated by the gram-scale reaction and derivatization of the product. Experimental results have confirmed Pd and Bi played critical roles in the transformation and indicated the transformation might proceed via 2-halo-6-nitrobenzoic acid derivative intermediate.
Pteridinone derivatives as PI3-kinases inhibitors
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Page/Page column 13, (2008/12/07)
New compounds of formula 1 are provided which by virtue of their pharmaceutical activity as PI3-kinase modulators may be used in the therapeutic field for the treatment of inflammatory or allergic diseases. Examples of these include inflammatory and allergic respiratory complaints, inflammatory diseases of the gastro-intestinal tract and motor apparatus, inflammatory and allergic skin diseases, inflammatory eye diseases, diseases of the nasal mucosa, inflammatory or allergic conditions involving autoimmune reactions or inflammations of the kidney.
