1031685-28-5 Usage
Uses
Used in Pharmaceutical Industry:
2,4-Imidazolidinedione, 5-(3-bromophenyl)-1,3-bis(1,1-dimethylethyl)is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to facilitate the creation of complex molecular structures that can target specific biological pathways.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4-Imidazolidinedione, 5-(3-bromophenyl)-1,3-bis(1,1-dimethylethyl)is utilized as a component in the development of new pesticides and herbicides, leveraging its reactivity to form compounds with potent biological activity against pests and weeds.
Used in Specialty Chemicals Production:
2,4-Imidazolidinedione, 5-(3-bromophenyl)-1,3-bis(1,1-dimethylethyl)is employed as a specialty chemical intermediate, contributing to the production of high-value compounds used in niche applications such as high-performance materials and advanced coatings.
Used in Organic Synthesis Research:
2,4-Imidazolidinedione, 5-(3-bromophenyl)-1,3-bis(1,1-dimethylethyl)is also used as a research tool in organic synthesis, where its unique structure allows chemists to explore new reaction pathways and develop innovative synthetic methods for creating novel organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 1031685-28-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,1,6,8 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1031685-28:
(9*1)+(8*0)+(7*3)+(6*1)+(5*6)+(4*8)+(3*5)+(2*2)+(1*8)=125
125 % 10 = 5
So 1031685-28-5 is a valid CAS Registry Number.
1031685-28-5Relevant academic research and scientific papers
A Cu(I)-catalyzed C-H α-amination of esters. Direct synthesis of hydantoins
Zhao, Baoguo,Du, Haifeng,Shi, Yian
, p. 7220 - 7221 (2008/12/20)
This paper describes a novel intermolecular α-amination process of esters using CuCl as catalyst and di-tert-butyldiaziridinone as nitrogen source. A variety of hydantoins can be formed effectively under mild reaction conditions. Copyright
