404582-98-5 Usage
Uses
Used in Organic Synthesis:
ETHYL R-2-ACETYLTHIO-3-PHENYLPROPIONATE is used as a key intermediate in the synthesis of various organic compounds. Its reactivity allows it to participate in a range of chemical transformations, such as condensation, substitution, and rearrangement reactions, which are crucial for the production of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, ETHYL R-2-ACETYLTHIO-3-PHENYLPROPIONATE is utilized as a building block for the development of new drug candidates. Its ability to form diverse chemical entities makes it a valuable component in the creation of novel therapeutic agents with potential applications in treating various diseases and medical conditions.
Used in Agrochemical Industry:
ETHYL R-2-ACETYLTHIO-3-PHENYLPROPIONATE also finds application in the agrochemical sector, where it serves as a precursor for the synthesis of new pesticides and herbicides. Its involvement in the development of these agrochemicals contributes to enhancing crop protection and increasing agricultural productivity.
Used in Specialty Chemicals:
In the specialty chemicals market, ETHYL R-2-ACETYLTHIO-3-PHENYLPROPIONATE is employed as a versatile component in the production of various high-value chemicals. Its unique properties enable it to be incorporated into a wide array of applications, such as fragrances, dyes, and other specialty products that cater to specific industrial needs.
Check Digit Verification of cas no
The CAS Registry Mumber 404582-98-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,4,5,8 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 404582-98:
(8*4)+(7*0)+(6*4)+(5*5)+(4*8)+(3*2)+(2*9)+(1*8)=145
145 % 10 = 5
So 404582-98-5 is a valid CAS Registry Number.
404582-98-5Relevant academic research and scientific papers
One-pot synthesis of α-bromoesters and ketones from β-ketoesters and diketones using supported reagents system
Aoyama, Tadashi,Takido, Toshio,Kodomari, Mitsuo
, p. 1873 - 1876 (2007/10/03)
A simple and efficient method has been developed for the synthesis of α-bromoesters and ketones from β-ketoesters and diketones in one pot using a supported reagents system, CuBr2/Al2O 3-Na2CO3/Al2O3, in which β-ketoester reacts first with CuBr2/Al2O3 and the product, α-bromo-β-ketoester, reacts with Na 2CO3/Al2O3 to give the final product, α-bromoesters in good yields.
Synthesis of optically pure (S)-2-acetylthio-3-benzenepropanoic acid via enzymatic resolution
Zhu, Jingyang,You, Li,Zhao, Shannon X,White, Brenda,Chen, Jason G,Skonezny, Paul M
, p. 7585 - 7587 (2007/10/03)
A method of synthesizing optically pure (S)-2-acetylthio-3-benzenepropanoic acid has been developed and good to excellent enantiomeric excess achieved via enzymatic resolution.
