29823-21-0 Usage
Description
8-BROMOOCTANOIC ACID ETHYL ESTER, also known as Ethyl 8-bromooctanoate, is an organic compound that serves as a valuable research reagent in the field of organic synthesis and other chemical processes. It is characterized by its unique chemical structure and properties, which make it a versatile compound for various applications.
Uses
Used in Organic Synthesis:
8-BROMOOCTANOIC ACID ETHYL ESTER is used as a research reagent for its role in organic synthesis. It is particularly valuable in the development and synthesis of new organic compounds, contributing to the advancement of chemical research and innovation.
Used in Chemical Processes:
In addition to its role in organic synthesis, 8-BROMOOCTANOIC ACID ETHYL ESTER is also utilized in various chemical processes. Its unique properties make it a useful component in the development and optimization of different chemical procedures, further expanding its applications in the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 29823-21-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,8,2 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 29823-21:
(7*2)+(6*9)+(5*8)+(4*2)+(3*3)+(2*2)+(1*1)=130
130 % 10 = 0
So 29823-21-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H19BrO2/c1-2-13-10(12)8-6-4-3-5-7-9-11/h2-9H2,1H3
29823-21-0Relevant articles and documents
Ti-catalyzed homolytic opening of ozonides: A sustainable C-C bond-forming reaction
Rosales, Antonio,Munoz-Bascon, Juan,Lopez-Sanchez, Cristobal,Alvarez-Corral, Miriam,Munoz-Dorado, Manuel,Rodriguez-Garcia, Ignacio,Oltra, J. Enrique
, p. 4171 - 4176 (2012/06/18)
The unprecedented homolytic opening of ozonides promoted and catalyzed by titanocene(III) is reported. This novel reaction proceeds at room temperature under neutral, mild conditions compatible with many functional groups and provides carbon radicals suitable to form C-C bonds via both homocoupling and cross-coupling processes. The procedure has been advantageously exploited for the straightforward synthesis of the natural product brittonin A.
