112595-55-8 Usage
Description
2,3-Dibromo-2-(4-bromophenyl)propionic Acid, with the CAS number 112595-55-8, is an off-white solid compound that is utilized in various organic synthesis processes. It is a halogenated derivative of propionic acid, featuring two bromine atoms at the 2nd and 3rd positions, and a 4-bromophenyl group attached to the 2nd carbon. This unique structure endows it with specific chemical properties that make it valuable in the synthesis of various organic compounds.
Uses
Used in Organic Synthesis:
2,3-Dibromo-2-(4-bromophenyl)propionic Acid is used as a synthetic intermediate for the production of various organic compounds. Its application in this field is due to its unique structure, which allows for further chemical reactions and modifications to create a wide range of products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,3-Dibromo-2-(4-bromophenyl)propionic Acid is used as a building block for the development of new drugs. Its specific chemical properties make it a valuable component in the synthesis of various pharmaceutical compounds, potentially leading to the discovery of novel therapeutic agents.
Used in Chemical Research:
2,3-Dibromo-2-(4-bromophenyl)propionic Acid is also utilized in chemical research as a model compound for studying the properties and reactivity of halogenated organic molecules. This helps researchers gain a deeper understanding of the underlying chemical mechanisms and potentially develop new synthetic strategies and methodologies.
Used in Material Science:
In the field of material science, 2,3-Dibromo-2-(4-bromophenyl)propionic Acid may be employed in the development of new materials with specific properties. Its unique structure and reactivity can contribute to the creation of materials with tailored characteristics, such as improved stability, enhanced functionality, or novel applications.
Check Digit Verification of cas no
The CAS Registry Mumber 112595-55-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,5,9 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 112595-55:
(8*1)+(7*1)+(6*2)+(5*5)+(4*9)+(3*5)+(2*5)+(1*5)=118
118 % 10 = 8
So 112595-55-8 is a valid CAS Registry Number.
112595-55-8Relevant articles and documents
Chloro/bromotrimethylsilane-Cu(NO3)2·3H2O: Safe and efficient reagent system for the decarboxylative ipso-nitration and dibromination of cinnamic acids
Roshandel, Sahar,Gurung, Laxman,Mathew, Thomas,Prakash, G.K. Surya
supporting information, p. 2842 - 2845 (2017/06/27)
Further synthetic potential of halotrimethylsilane-nitrate salt mixture is revealed. A mixture of TMSX-Cu(NO3)2·3H2O system is found to be an efficient reagent system for both the decarboxylative nitration (ipso-nitration) when X?=?Cl, and dibromination of cinnamic acids, with X?=?Br, under mild conditions. The reactions are safe and simple, affording the corresponding products (E)-β-nitrostyrenes, and anti-2,3-dibromo-3-phenylpropanoic acids in high yields with high selectivity in a relatively short time. Use of hazardous and toxic nitrating systems such as acetyl nitrate and brominating agents such as molecular bromine can be avoided.
Convenient synthesis of terminal alkynes from anti-3-aryl-2,3- dibromopropanoic acids using a K2CO3/DMSO system
Cheng, Xuezhi,Jia, Jun,Kuang, Chunxiang
experimental part, p. 2350 - 2354 (2012/02/03)
A convenient, efficient, and generally applicable method was developed for the synthesis of terminal alkynes from anti-3-aryl-2,3-dibromopropanoic acids in the presence of DMSO and K2CO3.
Stereoselective synthesis of (E)-β-arylvinyl bromides by microwave-induced reaction of anti-3-aryl-2,3-dibromopropanoic acids using an AgOAc-AcOH system
Kuang, Chunxiang,Senboku, Hisanori,Tokuda, Masao
, p. 637 - 642 (2007/10/03)
(E)-β-Arylvinyl bromides were stereoselectively prepared in high yields by microwave irradiation of the corresponding anti-3-aryl-2,3- dibromopropanoic acids in AcOH in the presence of AgOAc for 0.5-3.0 min. (E)-β-Arylvinyl bromides were stereoselectively prepared in high yields by microwave irradiation of the corresponding anti-3-aryl-2,3-dibromo-propanoic acids in AcOH in the presence of AgOAc for 0.5-3.0 min.
