172900-88-8 Usage
Description
5-Oxazolidinepropanoic acid, 3-[(1,1-dimethylethoxy)carbonyl]-4-[(2S)-2-[[4-methoxy-3-(3-methoxypropoxy)phenyl]methyl]-3-methylbutyl]-2,2-dimethyl-α-(1-methylethyl)-, (αS,4S,5S)is a complex organic compound with a unique and specific chemical structure. It is classified as an alpha-aminoketone and is derived from a combination of 1,1-dimethylethoxy, 4-methoxy-3-(3-methoxypropoxy)phenylmethyl, and 3-methylbutyl groups. 5-Oxazolidinepropanoic acid, 3-[(1,1-diMethylethoxy)carbonyl]-4-[(2S)-2-[[4-Methoxy-3-(3-Methoxypropoxy)phenyl]Methyl]-3-Methylbutyl]-2,2-diMethyl-α-(1-Methylethyl)-, (αS,4S,5S)contains various functional groups including oxazolidine, carboxylic acid, and methyl groups.
Uses
Used in Pharmaceutical Industry:
5-Oxazolidinepropanoic acid, 3-[(1,1-dimethylethoxy)carbonyl]-4-[(2S)-2-[[4-methoxy-3-(3-methoxypropoxy)phenyl]methyl]-3-methylbutyl]-2,2-dimethyl-α-(1-methylethyl)-, (αS,4S,5S)is used as a pharmaceutical intermediate for the synthesis of various drugs and medications. Its unique structure and functional groups make it a valuable building block in the development of new pharmaceutical compounds.
Used in Chemical Research:
5-Oxazolidinepropanoic acid, 3-[(1,1-diMethylethoxy)carbonyl]-4-[(2S)-2-[[4-Methoxy-3-(3-Methoxypropoxy)phenyl]Methyl]-3-Methylbutyl]-2,2-diMethyl-α-(1-Methylethyl)-, (αS,4S,5S)is also used in chemical research for studying the properties and reactions of complex organic molecules. Its unique structure and functional groups provide valuable insights into the behavior of similar compounds and contribute to the advancement of organic chemistry.
Used in Material Science:
5-Oxazolidinepropanoic acid, 3-[(1,1-dimethylethoxy)carbonyl]-4-[(2S)-2-[[4-methoxy-3-(3-methoxypropoxy)phenyl]methyl]-3-methylbutyl]-2,2-dimethyl-α-(1-methylethyl)-, (αS,4S,5S)can be used in the development of new materials with specific properties. Its unique structure and functional groups can be utilized to create materials with tailored characteristics for various applications in industries such as plastics, coatings, and adhesives.
Check Digit Verification of cas no
The CAS Registry Mumber 172900-88-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,9,0 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 172900-88:
(8*1)+(7*7)+(6*2)+(5*9)+(4*0)+(3*0)+(2*8)+(1*8)=138
138 % 10 = 8
So 172900-88-8 is a valid CAS Registry Number.
172900-88-8Relevant articles and documents
Structural modification of the P2′ position of 2,7-dialkyl- substituted 5(S)-amino-4(S)-hydroxy-8-phenyl-octanecarboxamides: The discovery of aliskiren, a potent nonpeptide human renin inhibitor active after once daily dosing in marmosets
Maibaum, Jürgen,Stutz, Stefan,G?schke, Richard,Rigollier, Pascal,Yamaguchi, Yasuchika,Cumin, Frédéric,Rahuel, Joseph,Baum, Hans-Peter,Cohen, Nissim-Claude,Schnell, Christian R.,Fuhrer, Walter,Gruetter, Markus G.,Schilling, Walter,Wood, Jeanette M.
, p. 4832 - 4844 (2008/03/12)
Due to its function in the rate limiting initial step of the renin-angiotensin system, renin is a particularly promising target for drugs designed to control hypertension, a growing risk to health worldwide. Despite vast efforts over more than two decades
DELTA-AMINO-GAMMA-HYDROXY-OMEGA-ARYL-ALKANOIC ACID AMIDES
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, (2008/06/13)
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