57775-06-1 Usage
Nitrile derivative
Functional group This compound contains a nitrile functional group (C≡N), which is a strong electron-withdrawing group that can participate in various chemical reactions.
Bromophenyl and methylpropane groups
Substituents The nitrile functional group is attached to a bromophenyl group (Br-C6H4) and a methylpropane group (CH3-CH2-CH2-), which provide the compound with its unique chemical properties.
Organic synthesis building block
Synthesis applications 2-(2-Bromophenyl)-2-methylpropanenitrile is commonly used in organic synthesis to construct various pharmaceuticals, agrochemicals, and other fine chemicals.
Reagent for bromine and nitrile group introduction
Chemical reactions This compound can be used as a reagent in chemical reactions to introduce bromine and nitrile groups into organic molecules, which can be important for the synthesis of target compounds with desired properties.
Potential applications in new materials
Material development 2-(2-Bromophenyl)-2-methylpropanenitrile may have potential applications in the development of new materials due to its unique chemical structure and properties.
Intermediate for complex organic compound synthesis
Synthesis applications The compound can also serve as an intermediate for the synthesis of more complex organic compounds, which can be further modified or functionalized to achieve desired properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 57775-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,7,7 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 57775-06:
(7*5)+(6*7)+(5*7)+(4*7)+(3*5)+(2*0)+(1*6)=161
161 % 10 = 1
So 57775-06-1 is a valid CAS Registry Number.
57775-06-1Relevant articles and documents
Diastereoselective Construction of Eight-Membered Carbocycles through Palladium-Catalyzed C(sp3)-H Functionalization
Wan, Bin,Lu, Zhuoer,Wu, Zhuo,Cheng, Cang,Zhang, Yanghui
supporting information, p. 1269 - 1274 (2021/03/03)
A palladium-catalyzed cross-coupling reaction of 2-alkylphenyl bromides with biphenylene has been developed. The reactions formed eight-membered carbocycles through C(sp3)-H activation and the formation of two C-C bonds, and the chiral products were obtai
VEGFR3 INHIBITORS
-
Page/Page column 144, (2014/03/22)
This invention relates to a compound of the formula (I): The invention also relates to processes for the preparation of the compound of the formula (I), pharmaceutical agents or compositions containing the compound or a method of using the compound for th
Pd-catalyzed intramolecular acylation of aryl bromides via C-H functionalization: A highly efficient synthesis of benzocyclobutenones
Alvarez-Bercedo, Paula,Flores-Gaspar, Areli,Correa, Arkaitz,Martin, Ruben
supporting information; experimental part, p. 466 - 467 (2010/03/25)
(Chemical Equation Presented) A new catalyst system for the intramolecular acylation of aldehydes with aryl bromides via C-H functionalization is described. The transformation is distinguished by a remarkable functional group tolerance and hence allows fo
