96557-30-1 Usage
Description
2-(2-Bromophenyl)acetaldehyde is a di-substituted benzene derivative characterized by the presence of a bromine atom and an aldehyde functional group attached to a phenyl ring. This organic compound serves as a versatile intermediate in the synthesis of a variety of complex organic molecules and pharmaceuticals.
Uses
Used in Pharmaceutical Industry:
2-(2-Bromophenyl)acetaldehyde is used as a key intermediate in the synthesis of various pharmaceutical compounds for the development of new drugs. Its unique structure allows for the formation of diverse chemical entities with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 2-(2-Bromophenyl)acetaldehyde is utilized as a building block for the preparation of a wide range of organic compounds, including phenanthrenes and other aromatic systems. Its reactivity and functional group compatibility make it a valuable component in the creation of complex molecular architectures.
Used in Chemical Research:
2-(2-Bromophenyl)acetaldehyde also finds application in chemical research, where it is employed as a model compound to study various reaction mechanisms and explore new synthetic methodologies. Its unique properties and reactivity provide insights into the behavior of similar compounds and contribute to the advancement of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 96557-30-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,5,5 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 96557-30:
(7*9)+(6*6)+(5*5)+(4*5)+(3*7)+(2*3)+(1*0)=171
171 % 10 = 1
So 96557-30-1 is a valid CAS Registry Number.
96557-30-1Relevant articles and documents
Intramolecular Anti-Carbolithiation of Alkynes: Stereo-Directing Effect of Lithium-Coordinating Substituents
Ly, Kim Uyen,Boussonnière, Anne,Castanet, Anne-Sophie
supporting information, (2022/01/19)
This paper presents the results of our investigations on the stereochemical course of intramolecular carbolithiation of alkynes. It is shown that the presence of a lithium-chelating propargylic substituent completely reverses the otherwise favored syn-pro
Peroxygenase-Catalysed Epoxidation of Styrene Derivatives in Neat Reaction Media
Alcalde, Miguel,Arends, Isabel W. C. E.,Hollmann, Frank,Paul, Caroline E.,Rauch, Marine C. R.,Tieves, Florian
, (2019/08/30)
Biocatalytic oxyfunctionalisation reactions are traditionally conducted in aqueous media limiting their production yield. Here we report the application of a peroxygenase in neat reaction conditions reaching product concentrations of up to 360 mM.
Construction of 1,3-Dithio-Substituted Tetralins by [1,5]-Alkylthio Group Transfer Mediated Skeletal Rearrangement
Hisano, Naoya,Kamei, Yuto,Kansaku, Yaoki,Yamanaka, Masahiro,Mori, Keiji
, p. 4223 - 4226 (2018/07/29)
A novel skeletal rearrangement involving a [1,5]-alkylthio group transfer/cyclization sequence is described. Treatment of benzylidene malonates having a thioketal moiety at the homobenzyl position with a catalytic amount of Sc(OTf)3 afforded alkylthio group rearranged adducts in good chemical yields. Detailed investigation of the reaction mechanism revealed that an intramolecular conjugate addition/ring opening sequence (not through-space transfer) is the key to achieving this reaction.
