850411-17-5 Usage
Description
(S)-3-[2-(3-Bromo-phenyl)-2-oxo-ethylsulfanyl]-2-tert-butoxycarbonylamino-propionic acid methyl ester is a complex chiral organic compound characterized by its unique molecular structure, which includes a sulfanyl group, a bromophenyl group, and a tert-butoxycarbonylamino-propionic acid methyl ester group. (S)-3-[2-(3-Bromo-phenyl)-2-oxo-ethylsulfanyl]-2-tert-butoxycarbonylamino-propionic acid methyl ester is known for its specific spatial arrangement of atoms, which makes it a valuable candidate in pharmaceutical research and drug development.
Uses
Used in Pharmaceutical Research:
(S)-3-[2-(3-Bromo-phenyl)-2-oxo-ethylsulfanyl]-2-tert-butoxycarbonylamino-propionic acid methyl ester is used as a research compound for its potential applications in the development of new medications. Its unique molecular structure and chiral properties make it a promising candidate for further study and experimentation in the pharmaceutical industry.
Used in Drug Development:
In the field of drug development, (S)-3-[2-(3-Bromo-phenyl)-2-oxo-ethylsulfanyl]-2-tert-butoxycarbonylamino-propionic acid methyl ester is utilized as a key component in organic synthesis. Its structural features suggest that it may play a crucial role in the creation of novel therapeutic agents, contributing to the advancement of medical treatments.
Used in Organic Synthesis:
(S)-3-[2-(3-Bromo-phenyl)-2-oxo-ethylsulfanyl]-2-tert-butoxycarbonylamino-propionic acid methyl ester is also employed as an intermediate in organic synthesis, where its specific spatial arrangement and functional groups can be exploited to synthesize a variety of complex molecules with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Chemical Research:
(S)-3-[2-(3-Bromo-phenyl)-2-oxo-ethylsulfanyl]-2-tert-butoxycarbonylamino-propionic acid methyl ester is used as a subject of study in chemical research to better understand its properties, reactivity, and potential interactions with other molecules. This knowledge can be applied to improve existing synthetic methods or develop new ones, ultimately contributing to the advancement of chemical science and technology.
Check Digit Verification of cas no
The CAS Registry Mumber 850411-17-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,4,1 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 850411-17:
(8*8)+(7*5)+(6*0)+(5*4)+(4*1)+(3*1)+(2*1)+(1*7)=135
135 % 10 = 5
So 850411-17-5 is a valid CAS Registry Number.
