74213-59-5 Usage
Uses
Used in Pharmaceutical Industry:
(2R,3R)-diethyl 2-acetoxy-3-bromosuccinate is used as an intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with specific therapeutic properties, making it a valuable component in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, (2R,3R)-diethyl 2-acetoxy-3-bromosuccinate serves as a key intermediate for the production of pesticides and other agrochemicals. Its role in these applications is to provide the necessary functional groups for the synthesis of effective and targeted agrochemical products.
Used in Research and Development:
(2R,3R)-diethyl 2-acetoxy-3-bromosuccinate is utilized in research and development for exploring its potential biological and pharmacological activities. Its unique stereochemistry and functional groups make it an interesting candidate for studying the mechanisms of action and interactions with biological systems.
Used as a Reagent in Organic Synthesis:
(2R,3R)-diethyl 2-acetoxy-3-broMosuccinate is also used as a valuable reagent for the preparation of chiral building blocks and other compounds with specific stereochemical characteristics. Its versatility in organic synthesis contributes to the development of new and innovative chemical compounds with various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 74213-59-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,1 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 74213-59:
(7*7)+(6*4)+(5*2)+(4*1)+(3*3)+(2*5)+(1*9)=115
115 % 10 = 5
So 74213-59-5 is a valid CAS Registry Number.
74213-59-5Relevant academic research and scientific papers
An improved preparation of the activity-based probe JPM-OEt and in situ applications
Chehade, Kareem A. H.,Baruch, Amos,Verhelst, Steven H. L.,Bogyo, Matthew
, p. 240 - 244 (2007/10/03)
A short, stereoselective synthesis of the general, cell permeable cathepsin probe JPM-OEt, is presented. The synthetic route is improved and described in more detail than previous reports for related compounds. This serves as a facile method for the synth
Stereoselective synthesis of optically active forms of δ-multistriatin, the attractant for european populations of the smaller european elm bark beet
Mori, Kenji,Iwasawa, Hiroko
, p. 87 - 90 (2007/10/02)
A stereoselective synthesis of highly optically pure enantiomers of δ-multistriatin [(1S,2S,4S,5R)-2,4-dimethyl-5-ethyl-6, 8-dioxabicyclo[3.2.1)octane and its antipode] was accomplished starting from tartaric acid enantiomers.
