93427-11-3 Usage
Uses
Used in Pharmaceutical Research:
1-(2-bromoethyl)-3,5-dimethylbenzene is used as a valuable precursor for the synthesis of various biologically active compounds, including pharmaceutical drugs. The presence of the bromoethyl group allows for the creation of a diverse range of molecules with potential therapeutic applications.
Used in Agrochemicals:
1-(2-bromoethyl)-3,5-dimethylbenzene is also employed in the synthesis of agrochemicals, where its unique structure can contribute to the development of new pesticides or other agricultural products that can enhance crop protection and yield.
Used in Organic Synthesis:
1-(2-bromoethyl)-3,5-dimethylbenzene serves as an important intermediate in the production of various chemical products. Its role in organic chemistry is significant, as it can be used to introduce the bromoethyl group into other molecules, expanding the scope of synthetic possibilities.
Used as a Reagent:
In addition to its applications in synthesis, 1-(2-bromoethyl)-3,5-dimethylbenzene is used as a reagent in organic reactions. Its ability to participate in a variety of chemical transformations makes it a versatile tool for researchers and chemists working in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 93427-11-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,4,2 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 93427-11:
(7*9)+(6*3)+(5*4)+(4*2)+(3*7)+(2*1)+(1*1)=133
133 % 10 = 3
So 93427-11-3 is a valid CAS Registry Number.
93427-11-3Relevant articles and documents
Solution and Flash Vacuum Pyrolyses of β-(3,5-Disubstituted-phenyl)ethanesulfonyl Azides. Sultam, Pyrindine, and Azepine Formation
Abramovitch, Rudolph A.,Holcomb, William D.,Thompson, W. Marshall,Wake, Shigeo
, p. 5124 - 5131 (2007/10/02)
The solution and flash vacuum pyrolyses of β-(3,5-disubstituted-phenyl)ethanesulfonyl azides are reported.When R = Me, FVP results suggest that the substituents stabilize the intermediate leading to the 3,4-dihydro-2,1-benzothiazepine 2,2-dioxide (6a).A n