1215077-69-2 Usage
Uses
Used in Pharmaceutical Synthesis:
(3-Bromophenyl) n-butylsulfoxide is utilized as an intermediate in the development of new drugs, making it a valuable component in medicinal chemistry. Its unique structure allows it to be a key building block in the creation of various pharmaceutical agents.
Used in Agrochemical Production:
In the agrochemical industry, (3-Bromophenyl) n-butylsulfoxide serves as an intermediate, contributing to the synthesis of compounds that are used in agricultural applications to protect crops and enhance yields.
Used in Organic Synthesis:
(3-Bromophenyl) n-butylsulfoxide is also employed in organic synthesis, where it can be a precursor to other complex organic molecules, showcasing its versatility in chemical reactions.
Used as a Chiral Building Block:
Due to its specific structure, (3-Bromophenyl) n-butylsulfoxide has potential as a chiral building block, which is important in the synthesis of enantiomerically pure compounds, a critical aspect in many chemical and pharmaceutical processes.
Used in Environmental and Health Research:
The properties and reactivity of (3-Bromophenyl) n-butylsulfoxide are of interest to researchers studying its potential impact on the environment and human health, ensuring that its applications are safe and sustainable.
Check Digit Verification of cas no
The CAS Registry Mumber 1215077-69-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,5,0,7 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1215077-69:
(9*1)+(8*2)+(7*1)+(6*5)+(5*0)+(4*7)+(3*7)+(2*6)+(1*9)=132
132 % 10 = 2
So 1215077-69-2 is a valid CAS Registry Number.
1215077-69-2Relevant academic research and scientific papers
Selective [5,5]-Sigmatropic Rearrangement by Assembly of Aryl Sulfoxides with Allyl Nitriles
Zhang, Lei,He, Jia-Ni,Liang, Yuchen,Hu, Mengjie,Shang, Li,Huang, Xin,Kong, Lichun,Wang, Zhi-Xiang,Peng, Bo
supporting information, p. 5316 - 5320 (2019/03/21)
Aromatic [5,5]-sigmatropic rearrangement is an appealing protocol for accessing 1,4-substituted arenes. However, such a protocol has not been well utilized in organic synthesis because of the difficulties in the synthesis of the substrates, selectivity issues, and limited substrate scope. Described herein is a new [5,5]-sigmatropic reaction utilizing readily available aryl sulfoxides and allyl nitriles. This reaction features mild reaction conditions, high chemo- and regioselectivity, excellent functional-group compatibility, and broad substrate scope. Computational studies suggest that the success of the reaction can be attributed to the selective electrophilic assembly of the rearrangement precursors, in which a linear -C=C=N- linkage favors [5,5]-sigmatropic rearrangement over the competitive [3,3]-sigmatropic rearrangement.
SULPHUR-LINKED COMPOUNDS FOR TREATING OPHTHALMIC DISEASES AND DISORDERS
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Page/Page column 118, (2010/04/30)
Provided are sulphur-linked compounds, pharmaceutical compositions thereof, and methods of treating ophthalmic diseases and disorders, such as age-related macular degeneration and Stargardt's Disease, using said compounds and compositions.
